>>>>X59796 ID X59796 standard; RNA; HUM; 3170 BP. XX AC X59796; XX SV X59796.1 XX DT 12-FEB-1992 (Rel. 30, Created) DT 24-JAN-1995 (Rel. 42, Last updated, Version 6) XX DE H.sapiens mRNA for cadherin-5 XX KW cadherin. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Mammalia; Eutheria; OC Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-3169 RA Suzuki S.; RT ; RL Submitted (16-MAY-1991) to the EMBL/GenBank/DDBJ databases. RL S. Suzuki, Doheny Eye Institute, 1355 San Pablo St, Los Angeles, CA 90033, RL USA XX RN [2] RP 1-3169 RX MEDLINE; 91283540. RA Suzuki S., Sano K., Tanihara H.; RT "Diversity of the cadherin family: evidence for eight new cadherins in RT nervous tissue"; RL Cell Regul. 2:261-270(1991). XX RN [3] RP 1-3170 RA Suzuki S.; RT ; RL Submitted (24-JAN-1995) to the EMBL/GenBank/DDBJ databases. RL S. Suzuki, Doheny Eye Institute, 1355 San Pablo St, Los Angeles, CA 90033, RL USA XX DR SWISS-PROT; P33151; CAD5_HUMAN. XX FH Key Location/Qualifiers FH FT source 1. .3170 FT /db_xref="taxon:9606" FT /organism="Homo sapiens" FT /dev_stage="fetus, 15-20 weeks" FT /tissue_type="brain" FT CDS 104. .2446 FT /db_xref="SWISS-PROT:P33151" FT /product="cadherin-5" FT /protein_id="CAA42468.1" FT /translation="MMLLATSGACLGLLAVAAVAAAGANPAQRDTHSLLPTHRRQKRDW FT IWNQMHIDEEKNTSLPHHVGKIKSSVSRKNAKYLLKGEYVGKVFRVDAETGDVFAIERL FT DRENISEYHLTAVIVDKDTGENLETPSSFTIKVHDVNDNWPVFTHRLFNASVPESSAVG FT TSVISVTAVDADDPTVGDHASVMYQILKGKEYFAIDNSGRIITITKSLDREKQARYEIV FT VEARDAQGLRGDSGTATVLVTLQDINDNFPFFTQTKYTFVVPEDTRVGTSVGSLFVEDP FT DEPQNRMTKYSILRGDYQDAFTIETNPAHNEGIIKPMKPLDYEYIQQYSFIVEATDPTI FT DLRYMSPPAGNRAQVIINITDVDEPPIFQQPFYHFQLKENQKKPLIGTVLAMDPDAARH FT SIGYSIRRTSDKGQFFRVTKKGDIYNEKELDREVYPWYNLTVEAKELDSTGTPTGKESI FT VQVHIEVLDENDNAPEFAKPYQPKVCENAVHGQLVLQISAIDKDITPRNVKFKFILNTE FT NNFTLTDNHDNTANITVKYGQFDREHTKVHFLPVVISDNGMPSRTGTSTLTVAVCKCNE FT QGEFTFCEDMAAQVGVSIQAVVAILLCILTITVITLLIFLRRRLRKQARAHGKSVPEIH FT EQLVTYDEEGGGEMDTTSYDVSVLNSVRRGGAKPPRPALDARPSLYAQVQKPPRHAPGA FT HGGPGEMAAMIEVKKDEADHDGDGPPYDTLHIYGYEGSESIAESLSSLGTDSSDSDVDY FT DFLNDWGPRFKMLAELYGSDPREELLY" XX SQ Sequence 3170 BP; 773 A; 962 C; 844 G; 588 T; 3 other; >>>>L22968 ID L22968 standard; DNA; HUM; 781 BP. XX AC L22968; XX SV L22968.1 XX DT 15-DEC-1993 (Rel. 38, Created) DT 02-JUL-1999 (Rel. 60, Last updated, Version 2) XX DE Homo sapiens acidic growth fibroblast growth factor (aFGF) gene DE sequence. XX KW acidic fibroblast growth factor. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Mammalia; Eutheria; OC Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-781 RA Chiu I.-M., Gilmore E.C., Liu Y., Payson R.A.; RT "Construction of a yeast artificial chromosome contig encompassing the RT human acidic fibroblast growth factor (aFGF) gene: Toward the cloning of RT the ANLL/MDS tumor suppressor gene"; RL Unpublished. XX FH Key Location/Qualifiers FH FT source 1. .781 FT /db_xref="taxon:9606" FT /germline FT /organism="Homo sapiens" FT /cell_type="lymphoblast" XX SQ Sequence 781 BP; 207 A; 179 C; 213 G; 182 T; 0 other; >>>>V00508 ID V00508 standard; DNA; HUM; 3919 BP. XX AC V00508; XX SV V00508.1 XX DT 09-JUN-1982 (Rel. 01, Created) DT 10-FEB-1999 (Rel. 58, Last updated, Version 3) XX DE Human gene for epsilon-globin. XX KW epsilon-globin; germ line; globin. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Mammalia; Eutheria; OC Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1640-3919 RX MEDLINE; 81064664. RA Baralle F.E., Shoulders C.C., Proudfoot N.J.; RT "The primary structure of the human epsilon-globin gene"; RL Cell 21:621-626(1980). XX RN [2] RP 1-2160 RX MEDLINE; 81053776. RA Baralle F.E., Shoulders C.C., Goodbourn S., Jeffreys A., Proudfoot N.J.; RT "The 5' flanking region of human epsilon-globin gene"; RL Nucleic Acids Res. 8:4393-4404(1980). XX DR SWISS-PROT; P02100; HBE_HUMAN. DR TRANSFAC; R03113; HS$EG_01. DR TRANSFAC; R03114; HS$EG_02. DR TRANSFAC; R03115; HS$EG_03. DR TRANSFAC; R03116; HS$EG_04. DR TRANSFAC; R03117; HS$EG_05. DR TRANSFAC; R03118; HS$EG_06. DR TRANSFAC; R03119; HS$EG_07. DR TRANSFAC; R03120; HS$EG_08. DR TRANSFAC; R03121; HS$EG_09. XX FH Key Location/Qualifiers FH FT source 1. .3919 FT /db_xref="taxon:9606" FT /organism="Homo sapiens" FT CDS join(2079. .2171,2294. .2515,3371. .3499) FT /db_xref="SWISS-PROT:P02100" FT /protein_id="CAA23766.1" FT /translation="MVHFTAEEKAAVTSLWSKMNVEEAGGEALGRLLVVYPWTQRFFDS FT FGNLSSPSAILGNPKVKAHGKKVLTSFGDAIKNMDNLKPAFAKLSELHCDKLHVDPENF FT KLLGNVMVIILATHFGKEFTPEVQAAWQKLVSAVAIALAHKYH" XX SQ Sequence 3919 BP; 1203 A; 703 C; 937 G; 1072 T; 4 other; >>>>X65923 ID X65923 standard; RNA; HUM; 518 BP. XX AC X65923; XX NI g31302 XX DT 13-MAY-1992 (Rel. 31, Created) DT 23-SEP-1993 (Rel. 37, Last updated, Version 10) XX DE H.sapiens fau mRNA XX KW fau gene. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Vertebrata; Mammalia; Eutheria; Primates; OC Catarrhini; Hominidae; Homo. XX RN [1] RP 1-518 RA Michiels L.M.R.; RT ; RL Submitted (29-APR-1992) to the EMBL/GenBank/DDBJ databases. RL L.M.R. Michiels, University of Antwerp, Dept of Biochemistry, RL Universiteisplein 1, 2610 Wilrijk, BELGIUM XX RN [2] RP 1-518 RX MEDLINE; 93368957. RA Michiels L., Van der Rauwelaert E., Van Hasselt F., Kas K., RA Merregaert J.; RT " fau cDNA encodes a ubiquitin-like-S30 fusion protein and is expressed RT as an antisense sequences in the Finkel-Biskis-Reilly murine sarcoma RT virus"; RL Oncogene 8:2537-2546(1993). XX DR SWISS-PROT; P35544; UBIM_HUMAN. DR SWISS-PROT; Q05472; RS30_HUMAN. XX FH Key Location/Qualifiers FH FT source 1. .518 FT /organism="Homo sapiens" FT /chromosome="11q" FT /tissue_type="placenta" FT /clone_lib="cDNA" FT /clone="pUIA 631" FT /map="13" FT misc_feature 57. .278 FT /note="ubiquitin like part" FT CDS 57. .458 FT /db_xref="PID:g31303" FT /db_xref="SWISS-PROT:P35544" FT /db_xref="SWISS-PROT:Q05472" FT /gene="fau" FT /translation="MQLFVRAQELHTFEVTGQETVAQIKAHVASLEGIAPEDQVVLLAG FT APLEDEATLGQCGVEALTTLEVAGRMLGGKVHGSLARAGKVRGQTPKVAKQEKKKKKTG FT RAKRRMQYNRRFVNVVPTFGKKKGPNANS" FT misc_feature 98. .102 FT /note="nucleolar localization signal" FT misc_feature 279. .458 FT /note="S30 part" FT polyA_signal 484. .489 FT polyA_site 509 XX SQ Sequence 518 BP; 125 A; 139 C; 148 G; 106 T; 0 other; >>>>K00650 ID K00650 standard; DNA; HUM; 6210 BP. XX AC K00650; M16287; XX NI g182734 XX DT 26-JUL-1991 (Rel. 28, Created) DT 15-NOV-1994 (Rel. 41, Last updated, Version 2) XX DE Human fos proto-oncogene (c-fos), complete cds. XX KW c-myc proto-oncogene; fos oncogene; proto-oncogene. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Vertebrata; Mammalia; Eutheria; Primates; OC Catarrhini; Hominidae; Homo. XX RN [1] RP 1-4165 RX MEDLINE; 83221560. RA van Straaten F., Muller R., Curran T., Van Beveren C., Verma I.M.; RT "Complete nucleotide sequence of a human c-onc gene: deduced amino acid RT sequence of the human c-fos protein"; RL Proc. Natl. Acad. Sci. U.S.A. 80:3183-3187(1983). XX RN [2] RX MEDLINE; 86028185. RA Treisman R.; RT "Transient accumulation of c-fos RNA following serum stimulation RT requires a conserved 5' element and c-fos 3' sequences"; RL Cell 42:889-902(1985). XX RN [3] RP 4166-6210 RX MEDLINE; 87217118. RA Verma I.M., Deschamps J., Van Beveren C., Sassone-Corsi P.; RT "Human fos gene"; RL Cold Spring Harb. Symp. Quant. Biol. 51:949-958(1986). XX DR CPGISLE; HSFOS; Release 3.0. DR GDB; 119917; FOS. DR SWISS-PROT; P01100; FOS_HUMAN. DR TFD; C00625; Release 7.0. DR TRANSFAC; R00458; HS$CFOS_01. DR TRANSFAC; R00459; HS$CFOS_02. DR TRANSFAC; R00460; HS$CFOS_03. DR TRANSFAC; R00461; HS$CFOS_04. DR TRANSFAC; R00463; HS$CFOS_06. DR TRANSFAC; R00464; HS$CFOS_07. DR TRANSFAC; R00465; HS$CFOS_08. DR TRANSFAC; R00466; HS$CFOS_09. DR TRANSFAC; R00467; HS$CFOS_10. DR TRANSFAC; R00468; HS$CFOS_11. DR TRANSFAC; R00470; HS$CFOS_13. DR TRANSFAC; R00471; HS$CFOS_14. DR TRANSFAC; R01640; HS$CFOS_15. DR TRANSFAC; R01889; HS$CFOS_16. DR TRANSFAC; R03425; HS$CFOS_17. DR TRANSFAC; R04046; HS$CFOS_18. DR TRANSFAC; R04047; HS$CFOS_19. DR TRANSFAC; T00123; T00123. XX CC [2] sites; promoter region. C-fos is the human cellular homolog of CC the v-fos oncogene of Finkel-Biskis-Jinkins murine osteosarcoma CC virus (FBJ-MuSV). [2] It was found that both human and murine c-fos CC genes contained an enhancer-like element in their 5' noncoding CC regions that was necessary for increased transcription following CC serum activation. The FBJ-MuSV v-fos oncogene contains a deletion CC relative to murine and human c-fos proto-oncogenes that causes CC complete divergence of the COOH terminal protein sequences encoded. CC That deletion corresponds to positions 3182-3285 inclusive of this CC sequence. The FBJ-MuSV v-fos sequence is more closely related to CC murine than human c-fos sequences. The FBJ-MuSV v-fos coding CC sequence ends at a 'tag' stop codon coresponding to positions CC 3434-2436 of this sequence [1]. [1] notes two alu repeats beginning CC aproximately 500 and 1700 nucleotides downstream of the last base CC in this sequence. A TATA box is located at positions 701-707. Two CC potential polyadenylation signals are present in the 3' CC untranslated region. NCBI gi: 182734 XX FH Key Location/Qualifiers FH FT source 1. .6210 FT /organism="Homo sapiens" FT misc_feature 402. .453 FT /note="transcriptional activator region [2]" FT prim_transcript 734. .>3329 FT /note="c-fos mRNA [1]" FT CDS join(889. .1029,1783. .2034,2466. .2573,2688. .3329) FT /codon_start=1 FT /db_xref="PID:g182735" FT /db_xref="SWISS-PROT:P01100" FT /note="c-fos protein; NCBI gi: 182735" FT /translation="MMFSGFNADYEASSSRCSSASPAGDSLSYYHSPADSFSSMGSPVN FT AQDFCTDLAVSSANFIPTVTAISTSPDLQWLVQPALVSSVAPSQTRAPHPFGVPAPSAG FT AYSRAGVVKTMTGGRAQSIGRRGKVEQLSPEEEEKRRIRRERNKMAAAKCRNRRRELTD FT TLQAETDQLEDEKSALQTEIANLLKEKEKLEFILAAHRPACKIPDDLGFPEEMSVASLD FT LTGGLPEVATPESEEAFTLPLLNDPEPKPSVEPVKSISSMELKTEPFDDFLFPASSRPS FT GSETARSVPDMDLSGSFYAADWEPLHSGSLGMGPMATELEPLCTPVVTCTPSCTAYTSS FT FVFTYPEADSFPSCAAAHRKGSSSNEPSSDSLSSPTLLAL" FT exon <889. .1029 FT /note="c-fos protein; G00-119-917" FT /number=1 FT /gene="FOS" FT /map="14q24.3" FT intron 1030. .1782 FT /note="c-fos intron A" FT exon 1783. .2034 FT /number=2 FT intron 2035. .2465 FT /note="c-fos intron B" FT exon 2466. .2573 FT /number=3 FT intron 2574. .2687 FT /note="c-fos intron C" FT exon 2688. .>3329 FT /note="c-fos protein" FT /number=4 XX SQ Sequence 6210 BP; 1497 A; 1571 C; 1619 G; 1523 T; 0 other; >>>>X51466 ID X51466 standard; RNA; HUM; 3075 BP. XX AC X51466; M30456; XX NI g31105 XX DT 28-JUN-1990 (Rel. 24, Created) DT 12-SEP-1993 (Rel. 36, Last updated, Version 8) XX DE Human mRNA for elongation factor 2 XX KW elongation factor; elongation factor 2. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Vertebrata; Mammalia; Eutheria; Primates; OC Catarrhini; Hominidae; Homo. XX RN [1] RP 1-3075 RA Scheit K.H.; RT ; RL Submitted (18-JAN-1990) to the EMBL/GenBank/DDBJ databases. RL Scheit K.H., MPI fuer Biophysikalische Chemie, 3400 Goettingen. XX RN [2] RP 1-3075 RX MEDLINE; 90121741. RA Rapp G.G., Klaudiny J.J., Hagendorff G.G., Luck M.M., Scheit K.K.; RT "Complete sequence of the coding region of human elongation factor RT 2(EF-2) by enzymatic amplification of cDNA from human ovarian granulosa RT cells"; RL Biol. Chem. Hoppe-Seyler 370:1071-1075(1989). XX DR GDB; 119104; EEF2. DR SWISS-PROT; P13639; EF2_HUMAN. XX CC See also for partial elongation factor 2 mRNA. XX CC Data kindly reviewed (16-JUL-1990) by Sheit K.H. XX CC entry is replaced by Z11692 XX FH Key Location/Qualifiers FH FT source 1. .3075 FT /organism="Homo sapiens" FT /dev_stage="adult" FT /tissue_type="ovary" FT /cell_type="granulosa" FT CDS 1. .2577 FT /db_xref="PID:g31106" FT /db_xref="SWISS-PROT:P13639" FT /product="elongation factor 2" FT /translation="MVNFTVDQIRAIMDKKANIRNMSVIAHVDHGKSTLTDSLVCKAGI FT IASARAGETRFTDTRKDEQERCITIKSTAISLFYELSENDLNFIKQSKDGAGFLINLID FT SPGHVDFSSEVTAALRVTDGALVVVDCVSGVCVQTETVLRQAIAERIKPVLMMNKMDRA FT LLELQLEPEELYQTFQRIVENVNVIISTYGEGESGPMGNIMIDPVLGTVGFGSGLHGWA FT FTLKQFAEMYVAKFAAKGEGQLGPAERAKKVEDMMKKLWGDRYFDPANGKFSKSATSPE FT GKKLPRTFCQLILDPIFKVFDAIMNFKKEETAKLIEKLDIKLDSEDKDKEGKPLLKAVM FT RRWLPAGDALLQMITIHLPSPVTAQKYRCELLYEGPPDDEAAMGIKSCDPKGPLMMYIS FT KMVPTSDKGRFYAFGRVFSGLVSTGLKVRIMGPNYTPGKKEDLYLKPIQRTILMMGRYV FT EPIEDVPCGNIVGLVGVDQFLVKTGTITTFEHAHNMRVMKFSVSPVVRVAVEAKNPADL FT PKLVEGLKRLAKSDPMVQCIIEESGEHIIAGAGELHLEICLKDLEEDHACIPIKKSDPV FT VSYRETVSEESNVLCLSKSPNKHNRLYMKARPFPDGLAEDIDKGEVSARQELKQRARYL FT AEKYEWDVAEARKIWCFGPDGTGPNILTDITKGVQYLNEIKDSVVAGFQWATKEGALCE FT ENMRGVRFDVHDVTLHADAIHRGGGQIIPTARRCLYASVLTAQPRLMEPIYLVEIQCPE FT QVVGGIYGVLNRKRGHVFEESQVAGTPMFVVKAYLPVNESFGFTADLRSNTGGQAFPQC FT VFDHWQILPGDPFDNSSRPSQVVAETRKRKGLKEGIPALDNFLDKL" XX SQ Sequence 3075 BP; 678 A; 906 C; 924 G; 567 T; 0 other; >>>>X07523 ID X07523 standard; RNA; HUM; 1658 BP. XX AC X07523; Y00716; XX NI g32492 XX DT 16-JUL-1988 (Rel. 16, Created) DT 31-MAR-1995 (Rel. 43, Last updated, Version 2) XX DE Human mRNA for truncated form of complement factor H XX KW complement factor H. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Vertebrata; Mammalia; Eutheria; Primates; OC Catarrhini; Hominidae; Homo. XX RN [1] RP 1-1658 RA Day A.J.; RT ; RL Submitted (03-MAY-1988) to the EMBL/GenBank/DDBJ databases. RL Day A.J., Dept. of Biochemistry, University of Oxford, MRC RL Immunochemistry Unit, South Parks Road, Oxford OX1 3QU . XX RN [2] RX MEDLINE; 88134059. RA Ripoche J., Day A.J., Harris T.J.R., Sim R.B.; RT "The complete amino acid sequence of human complement factor H"; RL Biochem. J. 249:593-602(1988). XX DR SPTREMBL; Q14570; Q14570. XX CC Data kindly reviewed (06-JUN-1988) by Day A.J. XX FH Key Location/Qualifiers FH FT source 1. .1658 FT /organism="Homo sapiens" FT /clone_lib="pat153/PvuII/8" FT /clone="B-38-1 tissue=liver" FT misc_feature 1. .1408 FT /note="seq. identical to full-length factor H" FT misc_feature <1. .73 FT /note="5'-UT region" FT sig_peptide 74. .127 FT /note="put. signal peptide" FT CDS 74. .1423 FT /db_xref="PID:g758073" FT /db_xref="SPTREMBL:Q14570" FT /product="complement factor H" FT /translation="MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEG FT TQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVF FT EYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAME FT PDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPIS FT QKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLR FT IKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENM FT RRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYN FT QNYGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSFTL" FT mat_peptide 128. .1420 FT /note="translated region" FT misc_feature 1409. .1420 FT /note="unique coding seq. not found in full-length factor FT H" FT misc_feature 1421. .1423 FT /note="stop codon" FT misc_feature 1424. .1658 FT /note="3'-UT region" FT misc_feature 1634. .1639 FT /note="pot. polyA signal" XX SQ Sequence 1658 BP; 513 A; 296 C; 383 G; 466 T; 0 other; >>>>D00596 ID D00596 standard; DNA; HUM; 18596 BP. XX AC D00596; XX SV D00596.1 XX DT 17-JUL-1991 (Rel. 28, Created) DT 27-OCT-1998 (Rel. 57, Last updated, Version 2) XX DE Homo sapiens gene for thymidylate synthase, exons 1, 2, 3, 4, 5, DE 6, 7, complete cds. XX KW thymidylate syntase. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Mammalia; Eutheria; OC Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-18596 RX MEDLINE; 91056070. RA Kaneda S., Nalbantoglu J., Takeishi K., Shimizu K., Gotoh O., Seno T., RA Ayusawa D.; RT "Structural and Functional Analysis of the Human Thymidylate Synthase RT Gene"; RL J. Biol. Chem. 265:20277-20284(1990). XX DR SWISS-PROT; P04818; TYSY_HUMAN. XX CC These data kindly submitted in computer readable form by: CC Sumiko Kaneda CC National Institute of Genetics CC 1111 Yata CC Mishima 411 CC Japan CC Phone: +81-559-72-2732 CC Fax: +81-559-71-3651 XX FH Key Location/Qualifiers FH FT source 1. .18596 FT /chromosome="18" FT /db_xref="taxon:9606" FT /sequenced_mol="DNA" FT /organism="Homo sapiens" FT /clone="lambdaHTS-1 and lambdaHTS-3" FT /map="18p11.32" FT repeat_unit 1. .148 FT /note="Alu sequence" FT repeat_unit 202. .477 FT /note="Alu sequence" FT prim_transcript 822. .16246 FT /note="thymidylate synthase mRNA and introns" FT prim_transcript 824. .16246 FT /note="thymidylate synthase mRNA and introns" FT prim_transcript 828. .16246 FT /note="thymidylate synthase mRNA and introns" FT prim_transcript 841. .16246 FT /note="thymidylate synthase mRNA and introns" FT repeat_unit 862. .889 FT /note="inverted repeat" FT repeat_unit 904. .993 FT /note="triple tandem repeats" FT CDS join(1001. .1205,2895. .2968,5396. .5570,11843. .11944, FT 13449. .13624,14133. .14204,15613. .15750) FT /db_xref="SWISS-PROT:P04818" FT /EC_number="2.1.1.45" FT /product="thymidylate synthase" FT /protein_id="BAA00472.1" FT /translation="MPVAGSELPRRPLPPAAQERDAEPRPPHGELQYLGQIQHILRCGV FT RKDDRTGTGTLSVFGMQARYSLRDEFPLLTTKRVFWKGVLEELLWFIKGSTNAKELSSK FT GVKIWDANGSRDFLDSLGFSTREEGDLGPVYGFQWRHFGAEYRDMESDYSGQGVDQLQR FT VIDTIKTNPDDRRIIMCAWNPRDLPLMALPPCHALCQFYVVNSELSCQLYQRSGDMGLG FT VPFNIASYALLTYMIAHITGLKPGDFIHTLGDAHIYLNHIEPLKIQLQREPRPFPKLRI FT LRKVEKIDDFKAEDFQIEGYNPHPTIKMEMAV" FT exon <1001. .1205 FT /number=1 FT intron 1206. .2894 FT /number=1 FT protein_bind 1660. .1665 FT /bound_moiety="Sp1" FT protein_bind 1890. .1895 FT /bound_moiety="Sp1" FT protein_bind 1895. .1900 FT /bound_moiety="Sp1" FT exon 2895. .2968 FT /number=2 FT intron 2969. .5395 FT /number=2 FT repeat_unit 3049. .3347 FT /note="Alu sequence" FT repeat_unit 4953. .5245 FT /note="Alu sequence" FT exon 5396. .5570 FT /number=3 FT intron 5571. .11842 FT /number=3 FT repeat_unit 5768. .9405 FT /note="L1 sequence" FT repeat_unit 10125. .10389 FT /note="reiterated motif of GGA/TGAT" FT exon 11843. .11944 FT /number=4 FT intron 11945. .13448 FT /number=4 FT repeat_unit 12135. .12397 FT /note="Alu sequence" FT repeat_unit 12567. .12743 FT /note="Alu sequence" FT repeat_unit 12807. .13084 FT /note="Alu sequence" FT exon 13449. .13624 FT /number=5 FT intron 13625. .14132 FT /number=5 FT repeat_unit 13875. .14010 FT /note="Alu sequence" FT exon 14133. .14204 FT /number=6 FT intron 14205. .15612 FT /number=6 FT repeat_unit 14531. .14832 FT /note="Alu sequence" FT exon 15613. .>15750 FT /number=7 FT polyA_signal 15934. .15939 FT polyA_signal 16228. .16233 FT repeat_unit 17262. .17553 FT /note="Alu sequence" XX SQ Sequence 18596 BP; 4521 A; 3991 C; 4479 G; 5605 T; 0 other; >>>>Z69719 ID Z69719 standard; DNA; HUM; 33760 BP. XX AC Z69719; XX SV Z69719.1 XX DT 26-FEB-1996 (Rel. 46, Created) DT 22-NOV-1999 (Rel. 61, Last updated, Version 3) XX DE Human DNA sequence from cosmid NFG9 from a contig from the tip DE of the short arm of chromosome 16, spanning 2Mb of 16p13.3. DE Contains Interleukin 9 Receptor Pseudogene, repeat polymorphism, DE ESTs, CpG islands and endogenous retroviral DNA. XX KW 16p13.3; CpG island; Interleukin 9 Receptor Pseudogene; KW repeat polymorphism. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Teleostomi; OC Euteleostomi; Mammalia; Eutheria; Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-33760 RA Kershaw J.; RT ; RL Submitted (22-FEB-1996) to the EMBL/GenBank/DDBJ databases. RL Sanger Centre, Hinxton, Cambridgeshire, CB10 1RQ, England. E-mail enquires: RL humquery@sanger.ac.uk XX CC IMPORTANT: This sequence is not the entire insert of clone CC NFG9. It may be shorter because we only sequence overlapping CC sections once, or longer because we arrange for a small CC overlap between neighbouring submissions. XX CC The true left end of clone NFG9 is at 1 in this sequence. CC The true left end of clone RA36 is at 25872. XX CC NFG9 is from a 280kb clone contig extending from the telomere of 16p. CC Higgs D.R., Flint J. unpublished. MRC Molecular Haematology Unit, CC Institute of Molecular Medicine, Oxford. CC NFG9 is from the library CV007K. Choo et al.,(1986) Gene 46. 277-286. XX FH Key Location/Qualifiers FH FT source 1. .33760 FT /chromosome="16" FT /db_xref="taxon:9606" FT /organism="Homo sapiens" FT /map="16p13.3" FT /clone_lib="CV007K" FT /clone="XX-CNFG9" FT misc_feature <1. .2455 FT /note="Interleukin 9 Receptor Pseudogene" FT misc_feature 18189. .18928 FT /note="expressed region - matched by multiple ESTs" FT misc_feature 19221. .20145 FT /note="expressed region - matched by multiple ESTs" FT misc_feature 21315. .21782 FT /note="expressed region - matched by multiple ESTs" FT misc_feature 25685. .27491 FT /note="expressed region - matched by multiple ESTs" FT misc_feature 15707. .16924 FT /note="putative CpG island" FT misc_feature 23690. .25856 FT /note="putative CpG island" FT misc_feature 3706. .4408 FT /note="match: M64936 retinoic acid-inducible endogenous FT retroviral DNA" FT misc_feature 6936. .7220 FT /note="match: Z24661 DNA segment containing (CA) repeat" FT repeat_region 4625. .4816 FT /note="2 copies of 96 mer 89 % conserved" FT repeat_region 7010. .7035 FT /note="13 copies of CA 100% conserved" FT /note="Polymorphic by comparison with Z24661" FT repeat_region 10544. .10565 FT /note="11 copies of 2 mer 100 % conserved" FT repeat_region 15151. .15180 FT /note="15 copies of 2 mer 100 % conserved" FT repeat_region 15470. .15509 FT /note="20 copies of 2 mer 90 % conserved" FT repeat_region 30618. .30801 FT /note="4 copies of 46 mer 81 % conserved" FT repeat_region 13518. .13568 FT /note="THE1B element fragment" FT repeat_region 13651. .13824 FT /note="THE1B element fragment" FT repeat_region 27971. .28069 FT /note="MIR2 element fragment" FT repeat_region 1. .62 FT /note="Alu repeat: matches 62. .1 of consensus" FT /partial FT repeat_region 518. .772 FT /note="Alu repeat: matches 272. .1 of consensus" FT /partial FT repeat_region 2181. .2337 FT /note="Alu repeat: matches 149. .308 of consensus" FT /partial FT repeat_region 2551. .2705 FT /note="Alu repeat: matches 308. .152 of consensus" FT /partial FT repeat_region 2706. .2858 FT /note="Alu repeat: matches 170. .1 of consensus" FT /partial FT repeat_region 3216. .3273 FT /note="Alu repeat: matches 84. .151 of consensus" FT /partial FT repeat_region 3274. .3565 FT /note="Alu repeat: matches 1. .308 of consensus" FT repeat_region 3567. .3704 FT /note="Alu repeat: matches 121. .255 of consensus" FT /partial FT repeat_region 6722. .7015 FT /note="Alu repeat: matches 1. .308 of consensus" FT repeat_region 9137. .9426 FT /note="Alu repeat: matches 1. .308 of consensus" FT repeat_region 10333. .10543 FT /note="Alu repeat: matches 40. .266 of consensus" FT /partial FT repeat_region 10593. .10883 FT /note="Alu repeat: matches 308. .1 of consensus" FT repeat_region 11224. .11514 FT /note="Alu repeat: matches 1. .308 of consensus" FT repeat_region 11566. .11851 FT /note="Alu repeat: matches 1. .308 of consensus" FT repeat_region 11852. .12100 FT /note="Alu repeat: matches 1. .266 of consensus" FT /partial FT repeat_region 12188. .12340 FT /note="Alu repeat: matches 308. .136 of consensus" FT /partial FT repeat_region 12341. .12629 FT /note="Alu repeat: matches 308. .1 of consensus" FT repeat_region 12660. .12952 FT /note="Alu repeat: matches 308. .1 of consensus" FT repeat_region 13224. .13517 FT /note="Alu repeat: matches 308. .1 of consensus" FT repeat_region 14433. .14723 FT /note="Alu repeat: matches 1. .308 of consensus" FT repeat_region 14859. .15150 FT /note="Alu repeat: matches 1. .308 of consensus" FT repeat_region 15182. .15469 FT /note="Alu repeat: matches 1. .308 of consensus" FT repeat_region 17007. .17048 FT /note="Alu repeat: matches 296. .254 of consensus" FT /partial FT repeat_region 17049. .17241 FT /note="Alu repeat: matches 210. .1 of consensus" FT /partial FT repeat_region 17421. .17510 FT /note="Alu repeat: matches 308. .216 of consensus" FT /partial FT repeat_region 17511. .17673 FT /note="Alu repeat: matches 178. .1 of consensus" FT /partial XX SQ Sequence 33760 BP; 8532 A; 9139 C; 9245 G; 6844 T; 0 other; >>>>AB000095 ID AB000095 standard; RNA; HUM; 2399 BP. XX AC AB000095; XX SV AB000095.1 XX DT 10-MAR-1998 (Rel. 54, Created) DT 10-MAR-1998 (Rel. 54, Last updated, Version 1) XX DE Homo sapiens mRNA for hepatocyte growth factor activator DE inhibitor, complete cds. XX KW hepatocyte growth factor activator inhibitor. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Mammalia; Eutheria; OC Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-2399 RA Denda K.; RT ; RL Submitted (24-DEC-1996) to the EMBL/GenBank/DDBJ databases. RL Kimitoshi Denda, Tokyo Institute of Technology, Department of Life Science; RL 4259 Nagatsuta, Midori-ku, Yokohama, Kanagawa 227, Japan RL (E-mail:kdenda@bio.titech.ac.jp, Tel:45-924-5702, Fax:45-924-5771) XX RN [2] RA Shimomura T., Denda K., Kitamura A., Kawaguchi T., Kito M., Kondo J., RA Kagaya S., Qin L., Takata H., Miyazawa K., Kitamura N.; RT "Hepatocyte growth factor activator inhibitor, a novel Kunitz-type serine RT protease inhibitor"; RL J. Biol. Chem. 272:6370-6376(1997). XX DR SPTREMBL; O43278; O43278. XX FH Key Location/Qualifiers FH FT source 1. .2399 FT /db_xref="taxon:9606" FT /sequenced_mol="cDNA to mRNA" FT /organism="Homo sapiens" FT CDS 176. .1717 FT /db_xref="SPTREMBL:O43278" FT /product="hepatocyte growth factor activator inhibitor" FT /protein_id="BAA25014.1" FT /translation="MAPARTMARARLAPAGIPAVALWLLCTLGLQGTQAGPPPAPPGLP FT AGADCLNSFTAGVPGFVLDTNASVSNGATFLESPTVRRGWDCVRACCTTQNCNLALVEL FT QPDRGEDAIAACFLINCLYEQNFVCKFAPREGFINYLTREVYRSYRQLRTQGFGGSGIP FT KAWAGIDLKVQPQEPLVLKDVENTDWRLLRGDTDVRVERKDPNQVELWGLKEGTYLFQL FT TVTSSDHPEDTANVTVTVLSTKQTEDYCLASNKVGRCRGSFPRWYYDPTEQICKSFVYG FT GCLGNKNNYLREEECILACRGVQGPSMERRHPVCSGTCQPTQFRCSNGCCIDSFLECDD FT TPNCPDASDEAACEKYTSGFDELQRIHFPSDKGHCVDLPDTGLCKESIPRWYYNPFSEH FT CARFTYGGCYGNKNNFEEEQQCLESCRGISKKDVFGLRREIPIPSTGSVEMAVAVFLVI FT CIVVVVAILGYCFFKNQRKDFHGHHHHPPPTPASSTVSTTEDTEHLVYNHTTRPL" FT polyA_signal 2379. .2384 XX SQ Sequence 2399 BP; 490 A; 777 C; 684 G; 448 T; 0 other; >>>>AB009062 ID AB009062 standard; DNA; HUM; 532 BP. XX AC AB009062; XX SV AB009062.1 XX DT 15-JAN-1999 (Rel. 58, Created) DT 24-MAR-1999 (Rel. 59, Last updated, Version 2) XX DE Homo sapiens HERG gene, exon 6. XX KW HERG. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Mammalia; Eutheria; OC Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-532 RA Tanaka T.; RT ; RL Submitted (21-NOV-1997) to the EMBL/GenBank/DDBJ databases. RL Toshihiro Tanaka, Institute of Medical Science, University of Tokyo, RL Laboratory of Molecular Medicine; 4-6-1 Shirokanedai, Minato-ku, Tokyo RL 108-8639, Japan (E-mail:toshitan@ims.u-tokyo.ac.jp, Tel:81-3-5449-5374, RL Fax:81-3-5449-5406) XX RN [2] RA Itoh T., Tanaka T., Nagai R., Kamiya T., Sawayama T., Nakayama T., RA Tomoike H., Sakurada H., Yazaki Y., Nakamura Y.; RT "Genomic organization and mutational analysis of HERG, a gene responsible RT for familial long QT syndrome"; RL Hum. Genet. 102:435-439(1998). XX DR SPTREMBL; Q12809; Q12809. XX FH Key Location/Qualifiers FH FT source 1. .532 FT /db_xref="taxon:9606" FT /sequenced_mol="DNA" FT /organism="Homo sapiens" FT exon 75. .503 FT /number=6 FT /gene="HERG" XX SQ Sequence 532 BP; 87 A; 187 C; 146 G; 112 T; 0 other; >>>>X03487 ID X03487 standard; DNA; HUM; 512 BP. XX AC X03487; XX SV X03487.1 XX DT 02-JUL-1986 (Rel. 09, Created) DT 04-APR-1995 (Rel. 43, Last updated, Version 2) XX DE Human apoferritin H gene exon 1 XX KW ferritin. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-512 RX MEDLINE; 86120367. RA Costanzo F., Colombo M., Staempfli S., Santoro C., Marone M., Frank R., RA Delius H., Cortese R.; RT "Structure of gene and pseudogenes of human apoferritin H"; RL Nucleic Acids Res. 14:721-736(1986). XX DR EPD; EP11112; HS_FRIH. DR SWISS-PROT; P02794; FRIH_HUMAN. XX FH Key Location/Qualifiers FH FT source 1. .512 FT /db_xref="taxon:9606" FT /organism="Homo sapiens" FT misc_feature 65. .70 FT /note="GGGCGG box" FT misc_feature 103. .108 FT /note="GGGCGG box" FT misc_feature 126. .131 FT /note="GGGCGG box" FT promoter 150. .154 FT /note="put. TATA box" FT mRNA 179. .500 FT /note="exon 1" FT CDS join(387. .500,X03488.1:50. .196,X03488.1:453. .578, FT X03488.1:674. .838) FT /db_xref="SWISS-PROT:P02794" FT /label=apoh_cds FT /product="apoferritin H subunit" FT /protein_id="CAA27205.1" FT /translation="MTTASTSQVRQNYHQDSEAAINRQINLELYASYVYLSMSYYFDRD FT DVALKNFAKYFLHQSHEEREHAEKLMKLQNQRGGRIFLQDIKKPDCDDWESGLNAMECA FT LHLEKNVNQSLLELHKLATDKNDPHLCDFIETHYLNEQVKAIKELGDHVTNLRKMGAPE FT SGLAEYLFDKHTLGDSDNES" FT intron 501. .>512 FT /note="intron I" XX SQ Sequence 512 BP; 80 A; 212 C; 152 G; 64 T; 4 other; >>>>X03488 ID X03488 standard; DNA; HUM; 1132 BP. XX AC X03488; XX SV X03488.1 XX DT 02-JUL-1986 (Rel. 09, Created) DT 04-APR-1995 (Rel. 43, Last updated, Version 2) XX DE Human apoferritin H gene exons 2-4 XX KW ferritin. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-1132 RX MEDLINE; 86120367. RA Costanzo F., Colombo M., Staempfli S., Santoro C., Marone M., Frank R., RA Delius H., Cortese R.; RT "Structure of gene and pseudogenes of human apoferritin H"; RL Nucleic Acids Res. 14:721-736(1986). XX DR SWISS-PROT; P02794; FRIH_HUMAN. XX FH Key Location/Qualifiers FH FT source 1. .1132 FT /db_xref="taxon:9606" FT /organism="Homo sapiens" FT intron <1. .49 FT /note="intron I" FT exon 50. .196 FT /note="apoferritin H subunit (aa 39-87) (exon 2)" FT /usedin=X03487:apoh_cds FT intron 197. .452 FT /note="intron II" FT exon 453. .578 FT /note="apoferritin H subunit (exon 3) (aa 88-129)" FT /usedin=X03487:apoh_cds FT intron 579. .673 FT /note="intron III" FT exon 674. .999 FT /note="exon 4" FT - 674. .838 FT /note="apoferritin H subunit (aa 130-183)" FT /usedin=X03487:apoh_cds FT intron 1000. .>1132 FT /note="intron IV" XX SQ Sequence 1132 BP; 315 A; 235 C; 250 G; 320 T; 12 other; >>>>AP000504 ID AP000504 standard; DNA; HUM; 100000 BP. XX AC AP000504; XX SV AP000504.1 XX DT 28-SEP-1999 (Rel. 61, Created) DT 30-MAR-2000 (Rel. 63, Last updated, Version 2) XX DE Homo sapiens genomic DNA, chromosome 6p21.3, HLA Class I region, section DE 3/20. XX KW . XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-100000 RA Hirakawa M., Yamaguchi H., Imai K., Shimada J.; RT ; RL Submitted (21-SEP-1999) to the EMBL/GenBank/DDBJ databases. RL Mika Hirakawa, Japan Science and Technology Corporation (JST), Advanced RL Databases Department; 5-3, Yonbancho, Chiyoda-ku, Tokyo 102-0081, Japan RL (E-mail:mika@tokyo.jst.go.jp, URL:http://www-alis.tokyo.jst.go.jp/, RL Tel:81-3-5214-8491, Fax:81-3-5214-8470) XX RN [2] RA Shiina S., Tamiya G., Oka A., Inoko H.; RT "Homo sapiens 2,229,817bp genomic DNA of 6p21.3 HLA class I region"; RL Unpublished. XX CC This sequence is conducted by Tokai University as a JST sequencing CC Team. CC Principal Investigator: Hidetoshi Inoko Ph.D CC Phone:+81-463-93-1121, Fax:+81-463-94-8884, CC The sequence is submitted by Human Genome Sequencing in ALIS CC project of JST CC Japan Science and Technology Corporation (JST) CC 5-3, Yonbancyo, Chiyoda-ku, Tokyo, 102-0081 Japan CC For further infomation about this sequences, please visit our CC sequence archive Web site (http://www-alis.tokyo.jst.go.jp/HGS/top. CC html) or send email to webmaster@www-alis.tokyo.jst.go.jp XX FH Key Location/Qualifiers FH FT source 1. .100000 FT /chromosome="6" FT /db_xref="taxon:9606" FT /sequenced_mol="DNA" FT /organism="Homo sapiens" FT /map="6p21.3" FT STS complement(27976. .28119) FT /note="142.3/142.5;The location is between each flanking FT site of PCR primers." FT /standard_name="D6S273" FT STS 27986. .28119 FT /note="AFM142xh6;Genethon Marker;The location is between FT each flanking site of PCR primers." FT /standard_name="D6S273" FT STS complement(56785. .57036) FT /note="WI-6920;The location is between each flanking site FT of PCR primers." FT /standard_name="D6S1938" FT STS 56833. .57013 FT /note="Cda0tg07;The location is between each flanking site FT of PCR primers." FT STS complement(56842. .56985) FT /note="stSG1709;The location is between each flanking site FT of PCR primers." FT STS complement(56851. .57019) FT /note="RH20292;The location is between each flanking site FT of PCR primers." FT STS complement(63189. .63342) FT /note="stSG2609;The location is between each flanking site FT of PCR primers." FT STS 71948. .72053 FT /note="SHGC-7078;The location is between each flanking site FT of PCR primers." FT /standard_name="D6S2007" FT STS complement(79567. .79695) FT /note="stSG8393;The location is between each flanking site FT of PCR primers." FT STS 85833. .85947 FT /note="TIGR-A007I39;The location is between each flanking FT site of PCR primers." XX SQ Sequence 100000 BP; 23515 A; 25717 C; 26015 G; 24753 T; 0 other; >>>>AF129756 ID AF129756 standard; DNA; HUM; 184666 BP. XX AC AF129756; XX SV AF129756.1 XX DT 12-MAR-1999 (Rel. 59, Created) DT 29-OCT-1999 (Rel. 61, Last updated, Version 2) XX DE Homo sapiens MSH55 gene, partial cds; and CLIC1, DDAH, G6b, G6c, G5b, G6d, DE G6e, G6f, BAT5, G5b, CSK2B, BAT4, G4, Apo M, BAT3, BAT2, AIF-1, 1C7, LST-1, DE LTB, TNF, and LTA genes, complete cds. XX KW . XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Primates; Catarrhini; Hominidae; Homo. XX RN [1] RP 1-184666 RA Rowen L., Madan A., Qin S., Shaffer T., James R., Ratcliffe A., Abbasi N., RA Dickhoff R., Loretz C., Madan A., Dors M., Young J., Lasky S., Hood L.; RT "Sequence of the human major histocompatibility complex class III region"; RL Unpublished. XX RN [2] RP 1-184666 RA Rowen L.; RT ; RL Submitted (22-FEB-1999) to the EMBL/GenBank/DDBJ databases. RL Department of Molecular Biotechnology, Box 357730 University of Washington, RL Seattle, WA 98195, USA XX RN [3] RP 1-184666 RA Rowen L.; RT ; RL Submitted (28-OCT-1999) to the EMBL/GenBank/DDBJ databases. RL Multimegabase Sequencing Center, University of Washington, PO Box 357730, RL Seattle, WA 98195, USA XX DR EPD; EP11158; HS_TNFA. DR EPD; EP11159; HS_TNFB. DR SPTREMBL; O00452; O00452. DR SPTREMBL; O14931; O14931. DR SPTREMBL; O95445; O95445. DR SPTREMBL; O95866; O95866. DR SPTREMBL; O95868; O95868. DR SPTREMBL; O95869; O95869. DR SPTREMBL; O95870; O95870. DR SPTREMBL; O95871; O95871. DR SPTREMBL; O95872; O95872. DR SPTREMBL; O95873; O95873. DR SPTREMBL; O95874; O95874. DR SPTREMBL; O95875; O95875. DR SPTREMBL; Q9UKS8; Q9UKS8. DR SPTREMBL; Q9UKS9; Q9UKS9. DR SPTREMBL; Q9UKT0; Q9UKT0. DR SPTREMBL; Q9UKT1; Q9UKT1. DR SWISS-PROT; O00299; CLI1_HUMAN. DR SWISS-PROT; O43196; MSH5_HUMAN. DR SWISS-PROT; O95865; DDH2_HUMAN. DR SWISS-PROT; O95867; NG24_HUMAN. DR SWISS-PROT; P01375; TNFA_HUMAN. DR SWISS-PROT; P13862; KC2B_HUMAN. DR SWISS-PROT; Q06643; TNFC_HUMAN. XX CC Sequencing Methodology: high redundancy shotgun using plasmid CC templates. Interspersed Repeats were identified with RepeatMasker CC (available from CC http://ftp.genome.washington.edu/RM/RepeatMasker.html). This CC sequence overlaps BAC 215O24, Accession AF134726 and cosmid M9A CC (AC004181), thereby joining to the 2 Mb HLA class I region. It CC also overlaps the entry found in Y14768. XX FH Key Location/Qualifiers FH FT source 1. .184666 FT /chromosome="6" FT /db_xref="taxon:9606" FT /note="Major histocompatibility complex class III region." FT /organism="Homo sapiens" FT /clone="BAC 201G24" FT /clone_lib="RPCI11" FT /map="6p21.3" FT repeat_region complement(517. .812) FT /rpt_family="AluSx" FT repeat_region 859. .1156 FT /rpt_family="AluSg" FT unsure 1087. .1130 FT /note="low quality data" FT repeat_region 1430. .1725 FT /rpt_family="AluSq" FT repeat_region complement(1774. .1984) FT /rpt_family="LINE2" FT repeat_region complement(2054. .2346) FT /rpt_family="AluSx" FT mRNA join(complement(9848. .10040),complement(9455. .9614), FT complement(8782. .8905),complement(7116. .7196), FT complement(6903. .6965),complement(6048. .6169), FT complement(5774. .5883),complement(5492. .5527), FT complement(4757. .4839),complement(<2638. .2683)) FT /note="Intron-exon boundaries defined in relation to FT AF048096." FT /product="MSH5" FT CDS join(complement(9455. .9601),complement(8782. .8905), FT complement(7116. .7196),complement(6903. .6965), FT complement(6048. .6169),complement(5774. .5883), FT complement(5492. .5527),complement(4757. .4839), FT complement(<2638. .2683)) FT /codon_start=1 FT /db_xref="SWISS-PROT:O43196" FT /note="mismatch repair; Intron-exon boundaries defined in FT relation to AF048096. MSH5 is the human ortholog to S. FT cerevisiae MSH5 gene" FT /product="MSH5" FT /protein_id="AAD18072.1" FT /translation="MASLGANPRRTPQGPRPGAASSGFPSPAPVPGPREAEEEEVEEEE FT ELAEIHLCVLWNSGYLGIAYYDTSDSTIHFMPDAPDHESLKLLQRVLDEINPQSVVTSA FT KQDENMTRFLGKLASQEHREPKRPEIIFLPSVDFGLEISKQRLLSGNYSFIPDAMTATE FT KILFLSSIIPFDCLLTVRALGGLLKFLGRRRIGVELEDYNVSVPILGFKKFMLTHLVNI FT DQDTYSVLQIFKSESHPSVYKVASGLKEGLSLFGILNRCHCKWGEKLL" FT repeat_region 2952. .3247 FT /rpt_family="AluY" FT repeat_region 3320. .3633 FT /rpt_family="AluSx" FT repeat_region 3674. .3957 FT /rpt_family="AluSq" FT repeat_region 3958. .3997 FT /rpt_family="(CA)n" FT repeat_region 4013. .4310 FT /rpt_family="AluY" FT repeat_region complement(4950. .5241) FT /rpt_family="AluSx" FT repeat_region complement(6221. .6295) FT /rpt_family="MIR" FT repeat_region 7419. .7493 FT /rpt_family="LINE2" FT repeat_region 7516. .7818 FT /rpt_family="AluSx" FT repeat_region 7920. .8351 FT /rpt_family="MSTB" FT repeat_region 8391. .8686 FT /rpt_family="AluSg" FT repeat_region complement(8687. .8731) FT /rpt_family="(CA)n" FT repeat_region complement(9088. .9388) FT /rpt_family="AluSx" FT repeat_region complement(9454. .9500) FT /rpt_family="(GGA)n" FT repeat_region 10481. .10541 FT /rpt_family="MIR" FT repeat_region complement(10814. .10907) FT /rpt_family="LINE2" FT repeat_region complement(10910. .10972) FT /rpt_family="(CA)n" FT repeat_region complement(10991. .11020) FT /rpt_family="AT_rich" FT repeat_region complement(12628. .12930) FT /rpt_family="AluSq" FT repeat_region 12960. .13116 FT /rpt_family="L143_5end" FT mRNA join(13554. .13810,15809. .15918,16111. .16236,16400. .16506, FT 17674. .17855,19069. .19477) FT /note="Intron-exon boundaries defined in relation to cDNA FT in U93205." FT /product="CLIC1" FT CDS join(13772. .13810,15809. .15918,16111. .16236,16400. .16506, FT 17674. .17855,19069. .19230) FT /codon_start=1 FT /db_xref="SWISS-PROT:O00299" FT /note="nuclear chloride ion channel protein; Intron-exon FT boundaries defined in relation to cDNA in U93205. This FT gene is also known as NCC27 and G6" FT /product="CLIC1" FT /protein_id="AAD18073.1" FT /translation="MAEEQPQVELFVKAGSDGAKIGNCPFSQRLFMVLWLKGVTFNVTT FT VDTKRRTETVQKLCPGGQLPFLLYGTEVHTDTNKIEEFLEAVLCPPRYPKLAALNPESN FT TAGLDIFAKFSAYIKNSNPALNDNLEKGLLKALKVLDNYLTSPLPEEVDETSAEDEGVS FT QRKFLDGNELTLADCNLLPKLHIVQVVCKKYRGFTIPEAFRGVHRYLSNAYAREEFAST FT CPDDEEIELAYEQVAKALK" FT repeat_region complement(14222. .14264) FT /rpt_family="(CA)n" FT repeat_region complement(14837. .14918) FT /rpt_family="(GAAA)n" FT unsure 15914. .15947 FT /note="low quality data" FT repeat_region 16767. .16930 FT /rpt_family="MIR" FT repeat_region complement(16933. .17231) FT /rpt_family="AluSx" FT repeat_region 17264. .17521 FT /rpt_family="AluSx" FT repeat_region 18471. .18762 FT /rpt_family="AluSx" FT mRNA join(20893. .21207,21327. .21426,21548. .21621,21780. .21899, FT 22380. .22529,22719. .23030) FT /note="Intron-exon boundaries defined by an EST contig." FT /product="DDAH" FT CDS join(20911. .21207,21327. .21426,21548. .21621,21780. .21899, FT 22380. .22529,22719. .22835) FT /codon_start=1 FT /db_xref="SWISS-PROT:O95865" FT /note="NG-dimethylarginine dimethylamino hydrolase homolog; FT Intron-exon boundaries defined by an EST contig including FT AA188111, AA311681 and AI080469. There is a mouse cDNA FT orthologue in AF004106. This protein is most similar to FT NG-dimethylarginine dimethyl amino hydrolase by BLAST X. FT BLAST N shows little nucleotide similarity with AB001915, FT the cDNA for this. This gene is also known as NG30 and FT G6a" FT /product="DDAH" FT /protein_id="AAD18074.1" FT /translation="MGTPGEGLGRCSHALIRGVPESLASGEGAGAGLPALDLAKAQREH FT GVLGGKLRQRLGLQLLELPPEESLPLGPLLGDTAVIQGDTALITRPWSPARRPEVDGVR FT KALQDLGLRIVEIGDENATLDGTDVLFTGREFFVGLSKWTNHRGAEIVADTFRDFAVST FT VPVSGPSHLRGLCGMGGPRTVVAGSSDAAQKAVRAMAVLTDHPYASLTLPDDAAADCLF FT LRPGLPGVPPFLLHRGGGDLPNSQEALQKLSDVTLVPVSCSELEKAGAGLSSLCLVLST FT RPHS" FT repeat_region 24446. .24741 FT /rpt_family="AluY" FT mRNA join(complement(26628. .>26688),complement(26086. .26433), FT complement(25840. .25930),complement(25445. .25485), FT complement(25228. .25307),complement(<24998. .25102)) FT /product="G6b" FT CDS join(complement(26628. .26688),complement(26086. .26433), FT complement(25840. .25930),complement(25445. .25485), FT complement(25228. .25307),complement(24998. .25102)) FT /codon_start=1 FT /db_xref="SPTREMBL:O95866" FT /note="unknown; This gene is predicted by Genscan. There FT are no BLAST N hits to ESTs or significant BLAST X hits. FT However, there might be an orthologue in the mouse sequence FT found in AF109905. This gene is also known as NG31" FT /product="G6b" FT /protein_id="AAD18075.1" FT /translation="MAVFLQLLPLLLSRAQGNPGASLDGRPGDRVNLSCGGVSHPIRWV FT WAPSFPACKGLSKGRRPILWASSSGTPTVPPLQPFVGRLRSLDSGIRRLELLLSAGDSG FT TFFCKGRHEDESRTVLHVLGDRTYCKAPGPTHGSVYPQLLIPLLGAGLVLGLGALGLVW FT WLHRRLPPQPIRPLPRFAPLVKTEPQRPVKEEEPKIPGDLDQEPSLLYADLDHLALSRP FT RRLSTADPADASTIYAVVV" FT repeat_region 26941. .27095 FT /rpt_family="AluJo" FT repeat_region complement(27208. .27494) FT /rpt_family="AluSc" FT mRNA join(28336. .28441,29866. .29976,30759. .31022) FT /note="Intron-exon boundaries defined in relation to ESTs FT H03135 and AA930440." FT /product="G6c" FT CDS join(28390. .28441,29866. .29976,30759. .30973) FT /codon_start=1 FT /db_xref="SWISS-PROT:O95867" FT /note="ly6 family member; Intron-exon boundaries defined in FT relation to ESTs H03135 and AA930440. The closest FT similarity found with BLAST X is to rat Ly-6 (lymphocyte FT differentiation) antigen. This gene is also known as NG24" FT /product="G6c" FT /protein_id="AAD18076.1" FT /translation="MKALMLLTLSVLLCWVSADIRCHSCYKVPVLGCVDRQSCRLEPGQ FT QCLTTHAYLGKMWVFSNLRCGTPEEPCQEAFNQTNRKLGLTYNTTCCNKDNCNSAGPRP FT TPALGLVFLTSLAGLGLWLLH" FT repeat_region complement(30111. .30197) FT /rpt_family="MIR" FT repeat_region 30234. .30532 FT /rpt_family="AluSx" FT mRNA join(complement(34655. .>34709),complement(34441. .34563), FT complement(<32150. .32488)) FT /note="Intron-exon boundaries defined in part by EST FT AA535815 and AA794551." FT /product="G6d" FT mRNA join(complement(34655. .>34709),complement(34441. .34563), FT complement(<32265. .32609)) FT /note="putative; contains alternative exon 3; based on FT AA535815" FT /product="G6d" FT CDS join(complement(34655. .34709),complement(34441. .34563), FT complement(32265. .32488)) FT /codon_start=1 FT /db_xref="SPTREMBL:O95868" FT /note="Ly6 family member; This is the orthologue to NG25 FT defined in mouse AF109905. Human EST AA535815 splices FT differently than mouse EST AA794551. No similarities to FT this gene are found using BLAST X" FT /product="G6d" FT /protein_id="AAD18077.1" FT /translation="MKPQFVGILLSSLLGAALGNRMRCYNCGGSPSSSCKEAVTTCGEG FT RPQPGLEQIKLPGNPPVTLIHQHPACVAAHHCNQVETESVGDVTYPAHRDCYLGDLCNS FT AVASHVAPAGILAAAATALTCLLPGLWSG" FT repeat_region 32600. .32780 FT /rpt_family="L1MC4" FT repeat_region complement(32804. .33099) FT /rpt_family="AluSp" FT repeat_region complement(33128. .33430) FT /rpt_family="AluJo" FT repeat_region complement(33437. .33755) FT /rpt_family="AluJb" FT repeat_region 33787. .33909 FT /rpt_family="L1MD3" FT repeat_region 33912. .34065 FT /rpt_family="L1MD3" FT repeat_region 34073. .34114 FT /rpt_family="(CA)n" FT repeat_region complement(34952. .34995) FT /rpt_family="MER64B" FT repeat_region complement(34998. .35400) FT /rpt_family="MER64" FT CDS join(36253. .36304,37276. .37401,37524. .>37729) FT /codon_start=1 FT /db_xref="SPTREMBL:Q9UKT1" FT /note="Intron-exon boundaries defined in relation to FT AJ245419" FT /product="G6e" FT /protein_id="AAF04398.1" FT /translation="MGTSSIFLCVLFLCGALGLTMSPARGRLRCYICGFTKPCHPVPTE FT CRDDEACGISIGTSVKKLPLKGPVPSARLCHLLAALLHSVAPLLRAGPVQHSRFPTAAH FT QPPRLPAPLCGQLRWERTPPPLAS" FT repeat_region complement(36823. .37113) FT /rpt_family="AluY" FT repeat_region complement(38187. .38239) FT /rpt_family="(CA)n" FT repeat_region complement(38967. .39071) FT /rpt_family="(GA)n" FT mRNA join(complement(43110. .43183),complement(42281. .42610), FT complement(41934. .42197),complement(39886. .40041), FT complement(<39645. .39715)) FT /note="This gene is predicted by Genscan. Only 1 EST FT (AA318501) matches part of the predicted CDS." FT /product="G6f" FT CDS join(complement(43110. .43161),complement(42281. .42610), FT complement(41934. .42197),complement(39886. .40041), FT complement(39645. .39715)) FT /codon_start=1 FT /db_xref="SPTREMBL:O95869" FT /note="unknown; The closest similarity to this gene by FT BLAST X is mouse immunoglobulin kappa chain. There is a FT mouse orthologue to this predicted gene that gives an FT in-frame translation, found in AF109905. This gene is also FT known as NG32" FT /product="G6f" FT /protein_id="AAD18078.1" FT /translation="MAVLFLLLFLCGTPQAADNMQAIYVALGEAVELPCPSPSTLHGDE FT HLSWFCSPAAGSFTTLVAQVQVGRPAPDPGKPGRESRLRLLGNYSLWLEGSKEEDAGRY FT WCAVLGQHHNYQNWRVYDVLVLKGSQLSARAADGSPCNVLLCSVVPSRRMDSVTWQEGK FT GPVRGRVQSFWGSEAALLLVCPGEGLSEPRSRRPRIIRCLMTHNKGVSFSLAASIDASP FT ALCAPSTGWDMPWILMLLLTMGQGVVILALSIVLWRQRVRGAPGRDASIPQFKPEIQVY FT ENIHLARLG" FT repeat_region 40237. .40456 FT /rpt_family="AluSx" FT repeat_region 40510. .40806 FT /rpt_family="AluSc" FT repeat_region 40820. .40996 FT /rpt_family="AluSg" FT repeat_region 41004. .41131 FT /rpt_family="AluSc" FT repeat_region complement(41132. .41423) FT /rpt_family="AluSp" FT repeat_region 41425. .41457 FT /rpt_family="(TAAAA)n" FT repeat_region 41713. .41903 FT /rpt_family="AluSq" FT repeat_region 43541. .43796 FT /rpt_family="AluSx" FT repeat_region 43797. .43825 FT /rpt_family="(GAAAA)n" FT repeat_region complement(44093. .44119) FT /rpt_family="AT_rich" FT repeat_region 44278. .44398 FT /rpt_family="FLAM_C" FT repeat_region 44399. .44695 FT /rpt_family="AluSc" FT repeat_region 44696. .44722 FT /rpt_family="(TAAA)n" FT repeat_region 44728. .45029 FT /rpt_family="AluSp" FT repeat_region 45046. .45334 FT /rpt_family="AluJb" FT repeat_region complement(45449. .45559) FT /rpt_family="L1MD2" FT repeat_region complement(45678. .45962) FT /rpt_family="AluJo" FT repeat_region complement(45963. .46046) FT /rpt_family="FLAM_C" FT repeat_region complement(46055. .46353) FT /rpt_family="AluSx" FT mRNA join(46759. .46912,47932. .47988,48720. .48786,49032. .49118, FT 53030. .53115,56637. .56710,56920. .57042,58151. .58265, FT 58389. .58490,59467. .59530,59942. .59991,60365. .60488, FT 60950. .61054,61283. .61346,61764. .61820,61966. .62028, FT 62169. .62245,62329. .62427,62525. .62571,62774. .63096) FT /note="Intron-exon boundaries defined in relation to a FT contig of ESTs." FT /product="BAT5" FT CDS join(46781. .46912,47932. .47988,48720. .48786,49032. .49118, FT 53030. .53115,56637. .56710,56920. .57042,58151. .58265, FT 58389. .58490,59467. .59530,59942. .59991,60365. .60488, FT 60950. .61054,61283. .61346,61764. .61820,61966. .62028, FT 62169. .62245,62329. .62427,62525. .62571,62774. .62857) FT /codon_start=1 FT /db_xref="SPTREMBL:O95870" FT /note="unknown; Intron-exon boundaries defined by an EST FT contig containing ESTs AA322366, H29422, AA323699, T09123, FT AA319071, AA352959, H70804, AA478983 and others. The FT closest match by BLASTX is to a hypothetical protein FT encoded by a gene named F37A4.1. This gene is also known FT as NG26" FT /product="BAT5" FT /protein_id="AAD18079.1" FT /translation="MAKLLSCVLGPRLYKIYRERDSERAPASVPETPTAVTAPHSSSWD FT TYYQPRALEKHADSILALASVFWSISYYSSPFAFFYLYRKGYLSLSKVVPFSHYAGTLL FT LLLAGVACLRGIGRWTNPQYRQFITILEATHRNQSSENKRQLANYNFDFRSWPVDFHWE FT EPSSRKESRGGPSRRGVALLRPEPLHRGTADTLLNRVKKLPCQITSYLVAHTLGRRMLY FT PGSVYLLQKALMPVLLQGQARLVEECNGRRAKLLACDGNEIDTMFVDRRGTAEPQGQKL FT VICCEGNAGFYEVGCVSTPLEAGYSVLGWNHPGFAGSTGVPFPQNEANAMDVVVQFAIH FT RLGFQPQDIIIYAWSIGGFTATWAAMSYPDVSAMILDASFDDLVPLALKVMPDSWRGLV FT TRTVRQHLNLNNAEQLCRYQGPVLLIRRTKDEIITTTVPEDIMSNRGNDLLLKLLQHRY FT PRVMAEEGLRVVRQWLEASSQLEEASIYSRWEVEEDWCLSVLRSYQAEHGPDFPWSVGE FT DMSADGRRQLALFLARKHLHNFEATHCTPLPAQNFQMPWHL" FT repeat_region complement(49315. .49444) FT /rpt_family="FLAM_C" FT repeat_region 49459. .49623 FT /rpt_family="L1ME3A" FT repeat_region 49637. .49930 FT /rpt_family="AluSg" FT repeat_region 50014. .50318 FT /rpt_family="AluSx" FT repeat_region 50319. .50486 FT /rpt_family="AluSx" FT repeat_region 50491. .50580 FT /rpt_family="L1ME1" FT repeat_region complement(50632. .50934) FT /rpt_family="AluY" FT repeat_region 51296. .51383 FT /rpt_family="LINE2" FT repeat_region 51392. .51577 FT /rpt_family="AluSq" FT repeat_region 52093. .52241 FT /rpt_family="LINE2" FT repeat_region complement(53411. .53712) FT /rpt_family="AluSq" FT repeat_region complement(53715. .53881) FT /rpt_family="AluSx" FT repeat_region complement(53882. .54179) FT /rpt_family="AluY" FT repeat_region complement(54180. .54314) FT /rpt_family="AluSx" FT repeat_region complement(54322. .54621) FT /rpt_family="AluSp" FT repeat_region complement(55024. .55162) FT /rpt_family="MIR" FT repeat_region 55373. .55674 FT /rpt_family="AluY" FT repeat_region 55718. .56011 FT /rpt_family="AluJo" FT repeat_region 57422. .57558 FT /rpt_family="MIR" FT repeat_region complement(58774. .58923) FT /rpt_family="MIR" FT repeat_region complement(59442. .59494) FT /rpt_family="L180_5end" FT repeat_region complement(63879. .64178) FT /rpt_family="AluSx" FT repeat_region complement(64253. .64279) FT /rpt_family="(CAAAA)n" FT repeat_region complement(64288. .64541) FT /rpt_family="AluSx" FT repeat_region complement(64552. .64851) FT /rpt_family="AluY" FT repeat_region 65341. .65645 FT /rpt_family="AluJb" FT mRNA join(<66034. .66086,69757. .69818,70803. .70970,72951. .73387) FT /note="Predicted by Genscan. Exon 4 confirmed by EST FT AI160056," FT /product="G5c" FT CDS join(66034. .66086,69757. .69818,70803. .70970,72951. .73114) FT /codon_start=1 FT /db_xref="SPTREMBL:O95871" FT /note="unknown; There is a mouse orthologue to this FT predicted gene in AF109905. This gene is also known as FT NG33" FT /product="G5c" FT /protein_id="AAD18080.1" FT /translation="MQTFPVAGALDPAILDTSSPQALYTVLLIVLVMMSLVFGKFVPVN FT WEPPQPLPFPKYLRCYRCLLETKELGCLLGSDICLTPAGSSCITLHKKNSSGSDVMVSD FT CRSKEQMSDCSNTRTSPVSGFWIFSQYCFLDFCNDPQNRGLYTP" FT repeat_region complement(66425. .66519) FT /rpt_family="(TGGA)n" FT repeat_region complement(67272. .67570) FT /rpt_family="AluSc" FT repeat_region complement(67685. .67987) FT /rpt_family="AluSx" FT repeat_region complement(67988. .68125) FT /rpt_family="AluSq" FT repeat_region 69068. .69326 FT /rpt_family="LINE2" FT repeat_region complement(70005. .70305) FT /rpt_family="AluSx" FT repeat_region complement(71089. .71374) FT /rpt_family="AluSx" FT unsure 71460. .71503 FT /note="low quality data" FT repeat_region complement(71882. .72060) FT /rpt_family="MIR" FT repeat_region complement(72419. .72496) FT /rpt_family="L1MC1" FT repeat_region complement(73713. .73993) FT /rpt_family="AluSx" FT repeat_region 74315. .74540 FT /rpt_family="L1ME3A" FT repeat_region 74580. .74696 FT /rpt_family="FLAM_A" FT repeat_region complement(75324. .75622) FT /rpt_family="AluSg" FT repeat_region complement(75625. .75920) FT /rpt_family="AluSp" FT repeat_region complement(76157. .76457) FT /rpt_family="AluSp" FT repeat_region complement(76798. .77088) FT /rpt_family="AluSx" FT repeat_region 77330. .77624 FT /rpt_family="AluSg" FT mRNA join(complement(78788. .79693),complement(77785. .78208)) FT /note="This gene is identified in AJ245417" FT /product="G5b" FT CDS join(complement(78788. .78809),complement(77790. .78208)) FT /codon_start=1 FT /db_xref="SPTREMBL:Q9UKT0" FT /note="unknown" FT /product="G5b" FT /protein_id="AAF04397.1" FT /translation="MVITIYYDVKVRFIVRGCGQYISYRCQEKRNTYFAEYWYQAQCCQ FT YNYCNSWSSPQLQSSLPEPHDRPLALPLSDSQIQWFYQALNLSLPLPNFHAGTEPDGLD FT PMVTLSLNLGLSFAELRRMYLFLNSSGLLVLPQAGLLTPHPS" FT repeat_region complement(78389. .78678) FT /rpt_family="AluJb" FT mRNA join(complement(83857. .83980),complement(83162. .83244), FT complement(82095. .82197),complement(81418. .81533), FT complement(80900. .80975),complement(80564. .80753), FT complement(80006. .80236)) FT /note="Intron-exon boundaries defined in relation to cDNA FT in X16312." FT /product="casein kinase II beta subunit" FT CDS join(complement(83162. .83233),complement(82095. .82197), FT complement(81418. .81533),complement(80900. .80975), FT complement(80564. .80753),complement(80146. .80236)) FT /codon_start=1 FT /db_xref="SWISS-PROT:P13862" FT /note="CSK2B" FT /product="casein kinase II beta subunit" FT /protein_id="AAD18081.1" FT /translation="MSSSEEVSWISWFCGLRGNEFFCEVDEDYIQDKFNLTGLNEQVPH FT YRQALDMILDLEPDEELEDNPNQSDLIEQAAEMLYGLIHARYILTNRGIAQMLEKYQQG FT DFGYCPRVYCENQPMLPIGLSDIPGEAMVKLYCPKCMDVYTPKSSRHHHTDGAYFGTGF FT PHMLFMVHPEYRPKRPANQFVPRLYGFKIHPMAYQLQLQAASNFKSPVKTIR" FT repeat_region complement(80384. .80444) FT /rpt_family="MIR" FT repeat_region 82634. .82931 FT /rpt_family="AluSx" FT repeat_region complement(82936. .83000) FT /rpt_family="MIR" FT mRNA join(85060. .85224,85488. .86212,87359. .87984) FT /note="Definition of the intron-exon boundaries for this FT gene is unclear. EST AA424367 supports exons 1 and 2. FT Comparison to mouse cDNA in L76155 supports exons 2 and 3." FT /product="BAT4" FT CDS join(85587. .86212,87359. .87803) FT /codon_start=1 FT /db_xref="SPTREMBL:O95872" FT /note="This is the in-frame translation that best FT corresponds to the mouse orthologue. However, the mouse FT CDS begins at an earlier start site (23 amino acids). This FT translation is most similar by BLAST X to an ankyrin motif FT in C. elegans (Z46934). This gene is also known as G5." FT /product="BAT4" FT /protein_id="AAD18082.1" FT /translation="MSRPLLITFTPATDPSDLWKDGQQQPQPEKPESTLDGAAARAFYE FT ALIGDESSAPDSQRSQTEPARERKRKKRRIMKAPAAEAVAEGASGRHGQGRSLEAEDKM FT THRILRAAQEGDLPELRRLLEPHEAGGAGGNINARDAFWWTPLMCAARAGQGAAVSYLL FT GRGAAWVGVCELSGRDAAQLAEEAGFPEVARMVRESHGETRSPENRSPTPSLQYCENCD FT THFQDSNHRTSTAHLLSLSQGPQPPNLPLGVPISSPGFKLLLRGGWEPGMGLGPRGEGR FT ANPIPTVLKRDQEGLGYRSAPQPRVTHFPAWDTRAVAGRERPPRVATLSWREERRREEK FT DRAWERDLRTYMNLEF" FT repeat_region 85782. .85869 FT /rpt_family="(GAA)n" FT repeat_region 86398. .86549 FT /rpt_family="MIR" FT repeat_region complement(86666. .86777) FT /rpt_family="HY1" FT repeat_region complement(86825. .86938) FT /rpt_family="AluSg" FT repeat_region 86961. .87121 FT /rpt_family="AluSx" FT repeat_region complement(87125. .87233) FT /rpt_family="FLAM_C" FT repeat_region complement(88351. .88650) FT /rpt_family="AluSp" FT repeat_region 89323. .89397 FT /rpt_family="GC_rich" FT mRNA 89929. .91292 FT /product="G4" FT CDS 90127. .91011 FT /codon_start=1 FT /db_xref="SPTREMBL:O95873" FT /note="unknown; This ORF is defined in relation to ESTs FT AA283116, AA282852, and AA826428, and by Genscan. There is FT an orthologue to this gene in mouse AF109719. See also FT AJ245433. This gene is also known as NG34" FT /product="G4" FT /protein_id="AAD18083.1" FT /translation="MFLRRLGGWLPRPWGRRKPMRPDPPYPEPRRVDSSSENSGSDWDS FT APETMEDVGHPKTKDSGALRVSRAASEPSKEEPQVEQLGSKRMDSLKWDQPISSTQESG FT RLEAGGASPKLRWDHVDSGGTRRPGVSPEGGLSVPGPGAPLEKPGRREKLLGWLRGEPG FT APSRYLGGPEECLQISTNLTLHLLELLASALLALCSRPLRAALDTLGLRGPLGLWLHGL FT LSFLAALHGLHAVLSLLTAHPLHFACLFGLLQALVLAVSLREPNGDEAATDWESEGLER FT EGEEQRGDPGKGL" FT mRNA join(complement(93995. .94412),complement(93449. .93603), FT complement(92777. .92850),complement(92597. .92695), FT complement(92352. .92450),complement(<91986. .92011)) FT /note="Intron-exon boundaries defined in relation to cDNA FT in AF118393." FT /product="Apo M" FT CDS join(complement(93995. .94108),complement(93449. .93603), FT complement(92777. .92850),complement(92597. .92695), FT complement(92352. .92450),complement(91986. .92011)) FT /codon_start=1 FT /db_xref="SPTREMBL:O95445" FT /note="NG20; apolipoprotein; This gene was annotated as FT NG20 in mouse AF109719. Subsequent to this, AF118393 FT suggests that the gene is a novel apolipoprotein. This FT gene is also known as NG20 and G3a, see AJ245434" FT /product="Apo M" FT /protein_id="AAD18084.1" FT /translation="MFHQIWAALLYFYGIILNSIYQCPEHSQLTTLGVDGKEFPEVHLG FT QWYFIAGAAPTKEELATFDPVDNIVFNMAAGSAPMQLHLRATIRMKDGLCVPRKWIYHL FT TEGSTDLRTEGRPDMKTELFSSSCPGGIMLNETGQGYQRFLLYNRSPHPPEKCVEEFKS FT LTSCLDSKAFLLTPRNQEACELSNN" FT unsure 92690. .92940 FT /note="low quality data" FT repeat_region complement(92913. .93210) FT /rpt_family="AluY" FT repeat_region 94836. .95124 FT /rpt_family="AluJb" FT repeat_region 95149. .95271 FT /rpt_family="MIR" FT repeat_region complement(95423. .95471) FT /rpt_family="AluJo" FT repeat_region complement(95501. .95668) FT /rpt_family="AluJb" FT repeat_region complement(95811. .96093) FT /rpt_family="AluSg1" FT repeat_region 96129. .96391 FT /rpt_family="AluJo" FT mRNA join(<97381. .97678,98296. .98414,100443. .100560, FT 100675. .100871,101106. .101159,101319. .101393, FT 102244. .102479,103546. .103675,104465. .104662, FT 104871. .105123,105467. .105544,105875. .105987, FT 106092. .106179,106957. .107243,107669. .107960, FT 108127. .108296,108480. .108533,108650. .108752, FT 108844. .108968,109134. .109280,109368. .109427, FT 109544. .109687,109766. .109873,110426. .110572, FT 110846. .111031) FT /note="Intron-exon boundaries defined in relation to cDNA FT in M33519 and EST AA406012, which gives a proper splice for FT exon 7." FT /product="BAT3" FT CDS join(97381. .97678,98296. .98414,100443. .100560, FT 100675. .100871,101106. .101159,101319. .101393, FT 102244. .102479,103546. .103675,104465. .104662, FT 104871. .105123,105467. .105544,105875. .105987, FT 106092. .106179,106957. .107243,107669. .107960, FT 108127. .108296,108480. .108533,108650. .108752, FT 108844. .108968,109134. .109280,109368. .109427, FT 109544. .109687,109766. .109873,110426. .110572, FT 110846. .110941) FT /codon_start=1 FT /db_xref="SPTREMBL:O95874" FT /note="unknown; This gene is also known as G3" FT /product="BAT3" FT /protein_id="AAD18085.1" FT /translation="MLKCPRIRSATHAGVVRSPGRQRWRLLGVLGSLPPRPAPARLALR FT NSLFGAADFLVVPHKSKAWGPGGSRKYRFEIPKYYRGNGSGRRWQVWGRPEVTVHLSAM FT EPNDSTSTAVEEPDSLEVLVKTLDSQTRTFIVGAQMNVKEFKEHIAASVSIPSEKQRLI FT YQGRVLQDDKKLQEYNVGGKVIHLVERAPPQTHLPSGASSGTGSASATHGGGSPPGTRG FT PGASVHDRNANSYVMVGTFNLPSDGSAVDVHINMEQAPIQSEPRVRLVMAQHMIRDIQT FT LLSRMECRGGPQPQHSQPPPQPPAVTPEPVALSSQTSEPVESEAPPREPMEAEEVEERA FT PAQNPELTPGPAPAGPTPAPETNAPNHPSPAEYVEVLQELQRLESRLQPFLQRYYEVLG FT AAATTDYNNNHEGREEDQRLINLVGESLRLLGNTFVALSDLRCNLACTPPRHLHVVRPM FT SHYTTPMVLQQAAIPIQINVGTTVTMTGNGTRPPPTPNAEAPPPGPGQASSVAPSSTNV FT ESSAEGAPPPGPAPPPATSHPRVIRISHQSVEPVVMMHMNIQDSGTQPGGVPSAPTGPL FT GPPGHGQTLGQQVPGFPTAPTRVVIARPTPPQARPSHPGGPPVSGTLQGAGLGTNASLA FT QMVSGLVGQLLMQPVLVAQGTPGMAPPPAPATASASAGTTNTATTAGPAPGGPAQPPPT FT PQPSMADLQFSQLLGNLLGPAGPGAGGSGVASPTITVAMPGVPAFLQGMTDFLQATQTA FT PPPPPPPPPPPPAPEQQTMPPPGSPSGGAGSPGGLGLESLSPEFFTSVVQGVLSSLLGS FT LGARAGSSESIAAFIQRLSGSSNIFEPGADGALGFFGALLSLLCQNFSMVDVVMLLHGH FT FQPLQRLQPQLRSFFHQHYLGGQEPTPSNIRMATHTLITGLEEYVRESFSLVQVQPGVD FT IIRTNLEFLQEQFNSIAAHVLHCTDSGFGARLLELCNQGLFECLALNLHCLGGQQMELA FT AVINGRIRRMSRGVNPSLVSWLTTMMGLRLQVVLEHMPVGPDAILRYVRRVGDPPQPLP FT EEPMEVQGAERASPEPQRENASPAPGTTAEEAMSRGPPPAPEGGSRDEQDGASAETEPW FT AAAVPPEWVPIIQQDIQSQRKVKPQPPLSDAYLSGMPAKRRKTMQGEGPQLLLSEAVSR FT AAKAAGARPLTSPESLSRDLEAPEVQESYRQQLRSDIQKRLQEDPNYSPQRFPNAQRAF FT ADDP" FT repeat_region complement(97710. .97761) FT /rpt_family="(CA)n" FT repeat_region complement(98512. .98813) FT /rpt_family="AluSx" FT repeat_region complement(99385. .99684) FT /rpt_family="AluSq" FT repeat_region complement(99951. .100250) FT /rpt_family="AluSx" FT repeat_region 101755. .102053 FT /rpt_family="AluSx" FT repeat_region 102868. .102997 FT /rpt_family="AluSq" FT repeat_region 102998. .103298 FT /rpt_family="AluY" FT repeat_region 103299. .103402 FT /rpt_family="AluSq" FT repeat_region 103784. .104083 FT /rpt_family="AluSx" FT repeat_region complement(106331. .106630) FT /rpt_family="AluSc" FT repeat_region complement(106634. .106929) FT /rpt_family="AluJo" FT repeat_region complement(107670. .107718) FT /rpt_family="(TGG)n" FT repeat_region complement(111164. .111470) FT /rpt_family="AluSg" FT mRNA join(complement(129214. .129252), FT complement(127171. .127345),complement(126162. .126339), FT complement(125711. .125810),complement(125549. .125621), FT complement(124757. .124900),complement(124460. .124611), FT complement(124200. .124279),complement(123909. .124051), FT complement(123209. .123299),complement(122873. .123089), FT complement(121832. .122306),complement(120737. .120927), FT complement(120226. .120523),complement(119270. .119480), FT complement(117079. .118932),complement(116424. .116692), FT complement(116082. .116212),complement(115706. .115835), FT complement(115514. .115599),complement(115094. .115318), FT complement(114799. .114939),complement(114606. .114677), FT complement(114322. .114489),complement(114022. .114104), FT complement(113652. .113862),complement(113463. .113561), FT complement(113126. .113338),complement(112935. .113029), FT complement(112747. .112837),complement(112311. .112625)) FT /note="Intron-exon boundaries defined in relation to cDNA FT in M33509." FT /product="BAT2" FT CDS join(complement(127171. .127282), FT complement(126162. .126339),complement(125711. .125810), FT complement(125549. .125621),complement(124757. .124900), FT complement(124460. .124611),complement(124200. .124279), FT complement(123909. .124051),complement(123209. .123299), FT complement(122873. .123089),complement(121832. .122306), FT complement(120737. .120927),complement(120226. .120523), FT complement(119270. .119480),complement(117079. .118932), FT complement(116424. .116692),complement(116082. .116212), FT complement(115706. .115835),complement(115514. .115599), FT complement(115094. .115318),complement(114799. .114939), FT complement(114606. .114677),complement(114322. .114489), FT complement(114022. .114104),complement(113652. .113862), FT complement(113463. .113561),complement(113126. .113338), FT complement(112935. .113029),complement(112747. .112837), FT complement(112485. .112625)) FT /codon_start=1 FT /db_xref="SPTREMBL:O95875" FT /note="unknown; This gene is also known as G2" FT /product="BAT2" FT /protein_id="AAD18086.1" FT /translation="MSDRSGPTAKGKDGKKYSSLNLFDTYKGKSLEIQKPAVAPRHGLQ FT SLGKVAIARRMPPPANLPSLKAENKGNDPNVSLVPKDGTGWASKQEQSDPKSSDASTAQ FT PPESQPLPASQTPASNQPKRPPAAPENTPLVPSGVKSWAQASVTHGAHGDGGRASSLLS FT RFSREEFPTLQAAGDQDKAAKERESAEQSSGPGPSLRPQNSTTWRDGGGRGPDELEGPD FT SKLHHGHDPRGGLQPSGPPQFPPYRGMMPPFMYPPYLPFPPPYGPQGPYRYPTPDGPSR FT FPRVAGPRGSGPPMRLVEPVGRPSILKEDNLKEFDQLDQENDDGWAGAHEEVDYTEKLK FT FSDEEDGRDSDEEGAEGHRDSQSASGEERPPEADGKKGNSPNSEPPTPKTAWAETSRPP FT ETEPGPPAPKPPLPPPHRGPAGNWGPPGDYPDRGGPPCKPPAPEDEDEAWRQRRKQSSS FT EISLAVERARRRREEEERRMQEERRAACAEKLKRLDEKFGAPDKRLKAEPAAPPAAPST FT PAPPPAVPKELPAPPAPPPASAPTPEKEPEEPAQAPPAQSTPTPGVAAAPTLVSGGGST FT SSTSSGSFEASPVEPQLPSKEGPEPPEEVPPPTTPPVPKVEPKGDGIGPTRQPPSQGLG FT YPKYQKSLPPRFQRQQQEQLLKQQQQHQWQQHQQGSAPPTPVPPSPPQPVTLGAVPAPQ FT APPPPPKALYPGALGRPPPMPPMNFDPRWMMIPPYVDPRLLQGRPPLDFYPPGVHPSGL FT VPRERSDSGGSSSEPFDRHAPAMLRERGTPPVDPKLAWVGDVFTATPAEPRPLTSPLRQ FT AADEDDKGMRSETPPVPPPPPYLASYPGFPENGAPGPPISRFPLEEPGPRPLPWPPGSD FT EVAKIQTPPPKKEPPKEETAQLTGPEAGRKPARGVGSGGQGPPPPRRESRTETRWGPRP FT GSSRRGIPPEEPGAPPRRAGPIKKPPPPTKVEELPPKPLEQGDETPKPPKPDPLKITKG FT KLGGPKETPPNGNLSPAPRLRRDYSYERVGPTSCRGRGRGEYFARGRGFRGTYGGRGRG FT ARSREFRSYREFRGDDGRGGGTGGPNHPPAPRGRTASETRSEGSEYEEIPKRRRQRGSE FT TGSETHESDLAPSDKEAPTPKEGTLTQVPLAPPPPGAPPSPAPARFTARGGRVFTPRGV FT PSRRGRGGGRPPPQVCPGWSPPAKSLAPKKPPTGPLPPSKEPLKEKLIPGPLSPVARGG FT SNGGSNVGMEDGERPRRRRHGRAQQQDKPPRFRRLKQERENAARGSEGKPSLTLPASAP FT APEEALTTVTVAPAPRRAAAKSPDLSNQNSDQANEEWETASESSDFTSERRGDKEAPPP FT VLLTPKAVGTPGGGGGGAVPGISAMSRGDLSQRAKDLSKRSFSSQRPGMERQNRRPGPG FT GKAGSSGSSSGGGGGGPGGRTGPGRGDKRSWPSPKNRSRPPEERPPGLPLPPPPPSSSA FT VFRLDQVIHSNPAGIQQALAQLSSRQGSVTAPGGHPRHKPGPPQAPQGPSPRPPTRYEP FT QRVNSGLSSDPHFEEPGPMVRGVGGTPRDSAGVSPFPPKRRERPPRKPELLQEESLPPP FT HSSGFLGSKPEGPGPQAESRDTGTEALTPHIWNRLHTATSRKSYRPSSMEPWMEPLSPF FT EDVAGTEMSQSDSGVDLSGDSQVSSGPCSQRSSPDGGLKGAAEGPPKRPGGSSPLNAVP FT CEGPPGSEPPRRPPPAPHDGDRKELPREQPLPPGPIGTERSQHTDRGTEPGPIRPSHRP FT GPPVQFGTSDKDSDLRLVVGDSLKAEKELTASVTEAIPVSRDWELLPSAAASAEPQSKN FT LDSGHCVPEPSSSGQRLYPEVFYGSAGPSSSQISGGAMDSQLHPNSGGFRPGTPSLHPY FT RSQPLYLPPGPAPPSALLSGVALKGQFLDFSTMQATELGKLPAGGVLYPPPSFLYSPAF FT CPSPLPDTSLLQVRQDLPSPSDFYSTPLQPGGQSGFLPSGAPAQQMLLPMVDSQLPVVN FT FGSLPPAPPPAPPPLSLLPVGPALQPPSLAVRPPPAPATRVLPSPARPFPASLGRAELH FT PVELKPFQDYQKLSSNLGGPGSSRTPPTGRSFSGLNSRLKATPSTYSGVFRTQRVDLYQ FT QASPPDALRWIPKPWERTGLPPREGPSRRAEEPGSRGDKEPGLPPPR" FT repeat_region complement(119034. .119162) FT /rpt_family="AluJb" FT repeat_region complement(119739. .120036) FT /rpt_family="AluSq" FT repeat_region complement(120473. .120525) FT /rpt_family="(CAG)n" FT repeat_region complement(121222. .121509) FT /rpt_family="AluSg" FT repeat_region complement(121510. .121624) FT /rpt_family="AluJo" FT repeat_region complement(122461. .122564) FT /rpt_family="FLAM_A" FT repeat_region complement(123499. .123800) FT /rpt_family="AluJo" FT repeat_region 124974. .125267 FT /rpt_family="AluSc" FT repeat_region 126512. .126806 FT /rpt_family="AluSp" FT repeat_region 128575. .128679 FT /rpt_family="(GAA)n" FT repeat_region complement(129125. .129177) FT /rpt_family="(CGG)n" FT repeat_region complement(130173. .130227) FT /rpt_family="AT_rich" FT repeat_region 130421. .130695 FT /rpt_family="AluSg" FT misc_feature 130479. .184666 FT /note="Overlap with GenBank entry Y14768." FT variation 130699 FT /note="201G24: a; Y14678: aaaaag" FT /replace="aaaaag" FT repeat_region 130706. .131000 FT /rpt_family="AluSp" FT variation 130994 FT /note="201G24: a; Y14768: aaaag" FT /replace="aaaag" FT repeat_region 131076. .131373 FT /rpt_family="AluSc" FT repeat_region 131397. .131523 FT /rpt_family="AluSx" FT variation 131746 FT /note="201G24: a; Y14768: g" FT /replace="g" FT repeat_region 131813. .131918 FT /rpt_family="LINE2" FT variation 131939. .131940 FT /note="201G24: tt; Y14768: t" FT /replace="t" FT repeat_region complement(131945. .132246) FT /rpt_family="AluSq" FT variation 132149 FT /note="201G24: c; Y14768: t" FT /replace="t" FT repeat_region complement(132331. .132625) FT /rpt_family="AluSp" FT variation 132331. .132332 FT /note="201G24: tt; Y14768: t" FT /replace="t" FT repeat_region complement(132689. .132763) FT /rpt_family="MIR" FT variation 132842 FT /note="201G24: t; Y14768: a" FT /replace="a" FT mRNA join(complement(134711. .134761), FT complement(134483. .134544),complement(134329. .134395), FT complement(133920. .133961),complement(133559. .133721), FT complement(133142. .133249)) FT /note="Intron-exon boundaries defined in relation to cDNA FT in U19713." FT /product="AIF-1" FT CDS join(complement(134711. .134735), FT complement(134483. .134544),complement(134329. .134395), FT complement(133920. .133961),complement(133559. .133721), FT complement(133165. .133249)) FT /codon_start=1 FT /db_xref="SPTREMBL:Q9UKS9" FT /note="anti-inflammatory factor; This gene is also known as FT G1" FT /product="AIF-1" FT /protein_id="AAD18087.1" FT /translation="MSQTRDLQGGKAFRLLKAQQEERLDEINKQFLDDPKYSSDEDLPS FT KLEGFKEKYMEFDLNGNGDIDIMSLKRMLEKLGVPKTHLELKKLIGEVSSGSGETFSYP FT DFLRMMLGKRSAILKMILMYEEKAREKEKPTGPPAKKAISELP" FT repeat_region 134049. .134117 FT /rpt_family="(GGA)n" FT variation 134530 FT /note="201G24: t; Y14768: c" FT /replace="c" FT variation 135555 FT /note="201G24: g; Y14768: a" FT /replace="a" FT repeat_region complement(135926. .136220) FT /rpt_family="AluSc" FT repeat_region complement(136340. .136484) FT /rpt_family="LINE2" FT variation 136464. .136465 FT /note="201G24: ta; Y14768: tca" FT /replace="tca" FT repeat_region 136497. .136796 FT /rpt_family="AluSg" FT variation 136857. .136861 FT /note="201G24: ttatt; Y14768: ctctactct" FT /replace="ctctactct" FT variation 136870. .136872 FT /note="201G24: tcc; Y14768: tc" FT /replace="tc" FT repeat_region complement(136887. .137186) FT /rpt_family="AluSx" FT repeat_region complement(137187. .137463) FT /rpt_family="AluSg" FT variation 137303 FT /note="201G24: t; Y14768: c" FT /replace="c" FT repeat_region 137495. .137661 FT /rpt_family="AluJo" FT repeat_region complement(137667. .137719) FT /rpt_family="LINE2" FT repeat_region complement(137720. .138020) FT /rpt_family="AluSg" FT repeat_region complement(138336. .138630) FT /rpt_family="AluSc" FT repeat_region 138758. .138785 FT /rpt_family="(GGA)n" FT repeat_region complement(139335. .139633) FT /rpt_family="AluY" FT repeat_region 139638. .140152 FT /rpt_family="MER21B" FT repeat_region 140299. .140379 FT /rpt_family="MER21B" FT repeat_region 140380. .140422 FT /rpt_family="(CA)n" FT repeat_region complement(140441. .140722) FT /rpt_family="AluJb" FT repeat_region complement(140731. .141025) FT /rpt_family="AluJo" FT variation 140744 FT /note="201G24: a; Y14768: t" FT /replace="t" FT repeat_region complement(141040. .141338) FT /rpt_family="AluY" FT repeat_region complement(141339. .141632) FT /rpt_family="AluY" FT repeat_region 141637. .141659 FT /rpt_family="AT_rich" FT repeat_region complement(141671. .141799) FT /rpt_family="LINE2" FT repeat_region complement(141809. .141850) FT /rpt_family="LINE2" FT repeat_region 141987. .142266 FT /rpt_family="AluSp" FT repeat_region complement(142631. .142790) FT /rpt_family="AluJb" FT repeat_region complement(142796. .143099) FT /rpt_family="AluSx" FT repeat_region complement(143114. .143328) FT /rpt_family="AluSg" FT repeat_region complement(143329. .143383) FT /rpt_family="AluYa5" FT repeat_region complement(143388. .143512) FT /rpt_family="AluSg" FT repeat_region complement(143516. .143815) FT /rpt_family="AluSc" FT repeat_region 143819. .143842 FT /rpt_family="AT_rich" FT repeat_region complement(144093. .144384) FT /rpt_family="AluSx" FT variation 144318 FT /note="201G24: t; Y14768: c" FT /replace="c" FT repeat_region complement(144420. .144472) FT /rpt_family="MER80" FT repeat_region complement(144575. .144871) FT /rpt_family="AluY" FT variation 144886 FT /note="201G24: g; Y14768: t" FT /replace="t" FT repeat_region complement(144972. .145256) FT /rpt_family="AluSg" FT variation 145198 FT /note="201G24: c: Y14768: g" FT /replace="g" FT variation 145361 FT /note="201G24: g; Y14768: a" FT /replace="a" FT repeat_region 145456. .145556 FT /rpt_family="(GA)n" FT variation 145509 FT /note="201G24: t; Y14768: c" FT /replace="c" FT repeat_region 145560. .145798 FT /rpt_family="AluSx" FT repeat_region 145831. .145872 FT /rpt_family="LINE2" FT repeat_region 145927. .146216 FT /rpt_family="MER35" FT repeat_region complement(146238. .146621) FT /rpt_family="LINE2" FT repeat_region 146655. .146781 FT /rpt_family="FLAM_A" FT repeat_region 146817. .147118 FT /rpt_family="AluSq" FT unsure 146832. .146932 FT /note="low quality data" FT repeat_region 147380. .147649 FT /rpt_family="L1MB8" FT variation 147507. .147508 FT /note="201G24: ca; Y14768: caa" FT /replace="caa" FT repeat_region 147650. .147777 FT /rpt_family="FLAM_C" FT repeat_region complement(147778. .148086) FT /rpt_family="AluY" FT variation 147778. .147779 FT /note="201G24: tt: Y14768: t" FT /replace="t" FT variation 147943. .147944 FT /note="201G24: tt; Y14768: t" FT /replace="t" FT variation 147977 FT /note="201G24: t; Y14768: c" FT /replace="c" FT repeat_region 148087. .148265 FT /rpt_family="AluJo" FT repeat_region 148267. .148480 FT /rpt_family="L1ME3" FT repeat_region 148491. .148792 FT /rpt_family="AluY" FT repeat_region 148855. .149149 FT /rpt_family="AluSq" FT variation 149129. .149130 FT /note="201G24: ca; Y14768: caa" FT /replace="caa" FT variation 149373 FT /note="201G24: t; Y14768: c" FT /replace="c" FT repeat_region 149554. .149856 FT /rpt_family="AluSx" FT repeat_region 149974. .150269 FT /rpt_family="AluSg" FT variation 150420 FT /note="201G24: a; Y14768: c" FT /replace="c" FT repeat_region complement(150750. .151049) FT /rpt_family="AluSq" FT repeat_region 151483. .151794 FT /rpt_family="AluJo" FT variation 151781. .151784 FT /note="201G24: caaa; Y14768: ca" FT /replace="ca" FT repeat_region 152000. .152298 FT /rpt_family="AluSx" FT repeat_region 152329. .152629 FT /rpt_family="AluSg" FT repeat_region 152646. .152880 FT /rpt_family="AluJo" FT repeat_region 153032. .153230 FT /rpt_family="TIGGER1" FT repeat_region complement(153231. .153391) FT /rpt_family="AluJo" FT repeat_region complement(153392. .153683) FT /rpt_family="AluSp" FT repeat_region 153716. .154006 FT /rpt_family="AluJb" FT repeat_region complement(154010. .154165) FT /rpt_family="FAM" FT repeat_region 154166. .154222 FT /rpt_family="TIGGER1" FT repeat_region 154223. .154523 FT /rpt_family="AluSx" FT variation 154415 FT /note="201G24: g; Y14768: a" FT /replace="a" FT repeat_region 154527. .154587 FT /rpt_family="TIGGER1" FT repeat_region complement(154602. .154831) FT /rpt_family="AluJb" FT variation 154616 FT /note="201G24: g; Y14768: t" FT /replace="t" FT repeat_region complement(154832. .155132) FT /rpt_family="AluY" FT variation 155080 FT /note="201G24: a; Y14768: g" FT /replace="g" FT repeat_region complement(155133. .155219) FT /rpt_family="AluSx" FT repeat_region complement(155267. .155562) FT /rpt_family="AluJo" FT repeat_region 155563. .155707 FT /rpt_family="TIGGER1" FT repeat_region complement(155710. .156010) FT /rpt_family="AluSp" FT variation 155714. .155715 FT /note="201G24: tt; Y14768: t" FT /replace="t" FT repeat_region 156013. .156119 FT /rpt_family="TIGGER1" FT repeat_region 156132. .156400 FT /rpt_family="AluJb" FT repeat_region 156399. .156674 FT /rpt_family="AluSx" FT variation 156634 FT /note="201G24: g; Y14768: a" FT /replace="a" FT repeat_region 156686. .156739 FT /rpt_family="(CA)n" FT variation 156688. .156689 FT /note="201G24: aa; Y14768: aacacaca" FT /replace="aacacaca" FT variation 156933 FT /note="201G24: c; Y14768: g" FT /replace="g" FT mRNA join(157081. .157387,159919. .160263,160412. .160519, FT 160869. .161150) FT /note="Intron-exon boundaries defined in relation to cDNA FT in AF031337. This gene has alternative splice forms." FT /product="1C7" FT CDS join(157345. .157387,159919. .160263,160412. .160519, FT 160869. .160978) FT /codon_start=1 FT /db_xref="SPTREMBL:O14931" FT /product="1C7" FT /protein_id="AAD18088.1" FT /translation="MAWMLLLILIMVHPGSCALWVSQPPEIRTLEGSSAFLPCSFNASQ FT GRLAIGSVTWFRDEVVPGKEVRNGTPEFRGRLAPLASSRFLHDHQAELHIRDVRGHDAS FT IYVCRVEVLGLGVGTGNGTRLVVEKEHPQLGAGTVLLLRAGFYAVSFLSVAVGSTVYYQ FT GKCLTWKGPRRQLPAVVPAPLPPPCGSSAHLLPPVPGG" FT repeat_region complement(157637. .157802) FT /rpt_family="AluSc" FT repeat_region complement(157803. .158098) FT /rpt_family="AluSx" FT repeat_region complement(158099. .158229) FT /rpt_family="AluSq" FT repeat_region complement(158244. .158532) FT /rpt_family="AluSx" FT variation 158490 FT /note="201G24: c; Y14768: t" FT /replace="t" FT repeat_region 158615. .158727 FT /rpt_family="MER5A" FT variation 158660. .158661 FT /note="201G24: ag; Y14768: agtcaaaaactcggggggtagg" FT /replace="agtcaaaaactcggggggtagg" FT repeat_region 158913. .159208 FT /rpt_family="AluSx" FT repeat_region complement(159426. .159726) FT /rpt_family="AluSg" FT variation 159791. .159792 FT /note="201G24: cc; Y14768: cac" FT /replace="cac" FT repeat_region complement(161159. .161195) FT /rpt_family="AT_rich" FT mRNA join(complement(163238. .163346), FT complement(162727. .162845),complement(162312. .162404), FT complement(161235. .161548)) FT /note="Intron-exon boundaries defined in relation to cDNA FT in AF000424." FT /product="LST-1" FT CDS join(complement(162727. .162729), FT complement(162312. .162404),complement(161369. .161548)) FT /codon_start=1 FT /db_xref="SPTREMBL:O00452" FT /product="LST-1" FT /protein_id="AAD18090.1" FT /translation="MIYVSTGAWGWAGSCFWQWSFCPPACVGCIEEHLLSWSQAQGSSE FT QELHYASLQRLPVPSSEGPDLRGRDKRGTKEDPRADYACIAENKPT" FT repeat_region complement(161606. .161653) FT /rpt_family="(GA)n" FT variation 161642 FT /note="201G24: t; Y14768: c" FT /replace="c" FT variation 161646 FT /note="201G24: c; Y14768: t" FT /replace="t" FT repeat_region complement(161664. .161793) FT /rpt_family="FLAM_A" FT repeat_region complement(161804. .161926) FT /rpt_family="(GA)n" FT repeat_region complement(161940. .162069) FT /rpt_family="(GA)n" FT variation 162430 FT /note="201G24: t; Y14768: g" FT /replace="g" FT variation 162692 FT /note="201G24: c; Y14768: t" FT /replace="t" FT repeat_region 162829. .162858 FT /rpt_family="MIR" FT repeat_region complement(164770. .165055) FT /rpt_family="AluJo" FT repeat_region complement(165257. .165552) FT /rpt_family="AluSx" FT repeat_region complement(165566. .165867) FT /rpt_family="AluSq" FT repeat_region 165902. .165997 FT /rpt_family="MIR" FT repeat_region 166027. .166319 FT /rpt_family="AluJb" FT repeat_region complement(166490. .166790) FT /rpt_family="AluSx" FT variation 166508. .166509 FT /note="201G24: tt; Y14768: ga" FT /replace="ga" FT variation 166756 FT /note="201G24: c; Y14768: g" FT /replace="g" FT repeat_region complement(166858. .166902) FT /rpt_family="(TAAA)n" FT repeat_region 167301. .167377 FT /rpt_family="MIR" FT mRNA join(167620. .167789,168186. .168231,168415. .168486, FT 168882. .169488) FT /note="Intron-exon boundaries defined in relation to cDNA FT in L11015." FT /product="lymphotoxin beta" FT CDS join(167628. .167789,168186. .168231,168415. .168486, FT 168882. .169336) FT /codon_start=1 FT /db_xref="SWISS-PROT:Q06643" FT /note="LTB" FT /product="lymphotoxin beta" FT /protein_id="AAD18089.1" FT /translation="MGALGLEGRGGRLQGRGSLLLAVAGATSLVTLLLAVPITVLAVLA FT LVPQDQGGLVTETADPGAQAQQGLGFQKLPEEEPETDLSPGLPAAHLIGAPLKGQGLGW FT ETTKEQAFLTSGTQFSDAEGLALPQDGLYYLYCLVGYRGRAPPGGGDPQGRSVTLRSSL FT YRAGGAYGPGTPELLLEGAETVTPVLDPARRQGYGPLWYTSVGFGGLVQLRRGERVYVN FT ISHPDMVDFARGKTFFGAVMVG" FT repeat_region complement(169024. .169066) FT /rpt_family="GC_rich" FT repeat_region complement(170465. .170756) FT /rpt_family="AluJo" FT repeat_region complement(170919. .171055) FT /rpt_family="FLAM_C" FT mRNA join(complement(174118. .174455), FT complement(173466. .173511),complement(173231. .173278), FT complement(171719. .172929)) FT /note="Intron-exon boundaries defined in relation to cDNA FT in X01394." FT /product="tumor necrosis factor" FT repeat_region 171994. .172068 FT /rpt_family="(TAAA)n" FT CDS join(complement(174118. .174303), FT complement(173466. .173511),complement(173231. .173278), FT complement(172508. .172929)) FT /codon_start=1 FT /db_xref="SWISS-PROT:P01375" FT /note="TNF" FT /product="tumor necrosis factor" FT /protein_id="AAD18091.1" FT /translation="MSTESMIRDVELAEEALPKKTGGPQGSRRCLFLSLFSFLIVAGAT FT TLFCLLHFGVIGPQREEFPRDLSLISPLAQAVRSSSRTPSDKPVAHVVANPQAEGQLQW FT LNRRANALLANGVELRDNQLVVPSEGLYLIYSQVLFKGQGCPSTHVLLTHTISRIAVSY FT QTKVNLLSAIKSPCQRETPEGAEAKPWYEPIYLGGVFQLEKGDRLSAEINRPDYLDFAE FT SGQVYFGIIAL" FT repeat_region complement(173653. .173823) FT /rpt_family="MER35" FT repeat_region complement(173870. .173918) FT /rpt_family="LINE2" FT repeat_region complement(173924. .174061) FT /rpt_family="(GA)n" FT mRNA join(complement(177599. .177646), FT complement(177204. .177311),complement(177012. .177117), FT complement(175726. .176764)) FT /note="Intron-exon boundaries defined in relation to cDNA FT in D00102." FT /product="lymphotoxin alpha" FT repeat_region 175958. .175981 FT /rpt_family="AT_rich" FT CDS join(complement(177204. .177302), FT complement(177012. .177117),complement(176352. .176764)) FT /codon_start=1 FT /db_xref="SPTREMBL:Q9UKS8" FT /note="LTA" FT /product="lymphotoxin alpha" FT /protein_id="AAD18092.1" FT /translation="MTPPERLFLPRVCGTTLHLLLLGLLLVLLPGAQGLPGVGLTPSAA FT QTARQHPKMHLAHSNLKPAAHLIGDPSKQNSLLWRANTDRAFLQDGFSLSNNSLLVPTS FT GIYFVYSQVVFSGKAYSPKATSSPLYLAHEVQLFSSQYPFHVPLLSSQKMVYPGLQEPW FT LHSMYHGAAFQLTQGDQLSTHTDGIPHLVLSPSTVFFGAFAL" FT variation 177038 FT /note="201G24: t; Y14768: g" FT /replace="g" FT repeat_region 177316. .177351 FT /rpt_family="(GA)n" FT variation 177393 FT /note="201G24: c; Y14768: g" FT /replace="g" FT repeat_region 177469. .177582 FT /rpt_family="(GA)n" FT variation 177509 FT /note="201G24: c; Y14768: t" FT /replace="t" FT variation 177681 FT /note="201G24: g; Y14768: t" FT /replace="t" FT variation 177751 FT /note="201G24: t; Y14768: c" FT /replace="c" FT variation 178054 FT /note="201G24: c; Y14768: t" FT /replace="t" FT repeat_region 178686. .178982 FT /rpt_family="AluSx" FT variation 178966. .178967 FT /note="201G24: ca; Y14768: caa" FT /replace="caa" FT repeat_region complement(179002. .179448) FT /rpt_family="L1ME2" FT repeat_region 179818. .180228 FT /rpt_family="MER39" FT repeat_region complement(180229. .180531) FT /rpt_family="AluSx" FT variation 180234. .180235 FT /note="201G24: ct; Y14768: cttt" FT /replace="cttt" FT repeat_region 180734. .181033 FT /rpt_family="AluY" FT misc_feature 180792. .184666 FT /note="Overlap with cosmid M9A (AC004181)." FT variation 181023 FT /note="201G24: c; M9A and Y14768: a" FT /replace="a" FT variation 181595 FT /note="201G24 and M9A: c; Y14768: t" FT /replace="t" FT repeat_region complement(181795. .182333) FT /rpt_family="LINE2" FT repeat_region complement(182342. .182382) FT /rpt_family="(CA)n" FT variation 182349. .182350 FT /note="201G24: gt; M9A: gtgcgtgcat" FT /replace="gtgcgtgcat" FT variation 182356. .182357 FT /note="201G24 and M9A: cg; Y14768: catgcgtgcgtgtgtg" FT /replace="catgcgtgcgtgtgtg" FT repeat_region 182388. .182433 FT /rpt_family="(GA)n" FT variation 182423. .182424 FT /note="201G24: ag; M9A and Y14768: a" FT /replace="a" FT repeat_region complement(182453. .182719) FT /rpt_family="AluJo" FT repeat_region complement(182720. .183015) FT /rpt_family="AluSq" FT variation 182732 FT /note="201G24: a; M9A and Y14768: t" FT /replace="t" FT repeat_region complement(183017. .183057) FT /rpt_family="FLAM_C" FT repeat_region complement(183070. .183368) FT /rpt_family="AluSx" FT variation 183368. .183369 FT /note="201G24: ct; M9A and Y14768: ctttt" FT /replace="ctttt" FT repeat_region complement(183369. .183665) FT /rpt_family="AluSx" FT variation 183597 FT /note="201G24: c; M9A and Y14768: t" FT /replace="t" FT repeat_region complement(183669. .183822) FT /rpt_family="FRAM" FT variation 183789. .183790 FT /note="201G24: ca; M9A and Y14768: caaa" FT /replace="caaa" FT repeat_region complement(183833. .184125) FT /rpt_family="AluSg" FT variation 183931 FT /note="210G24: c; M9A and Y14768: t" FT /replace="t" FT repeat_region complement(184218. .184319) FT /rpt_family="LINE2" FT repeat_region complement(184316. .184524) FT /rpt_family="LINE2" FT variation 184423 FT /note="201G24: t; M9A and Y14768: c" FT /replace="c" XX SQ Sequence 184666 BP; 43878 A; 47035 C; 47743 G; 46010 T; 0 other;