Dbfetch
ID AM850137; SV 1; linear; genomic DNA; STD; HUM; 2676 BP. XX AC AM850137; XX DT 11-OCT-2007 (Rel. 93, Created) DT 10-JUN-2009 (Rel. 101, Last updated, Version 3) XX DE Homo sapiens HLA-B gene for MHC class I antigen, HLA-B*44new allele, exons DE 1-3 XX KW HLA-B gene; HLA-B*44new allele; human leucocyte antigen B; KW major histocompatibility complex; MHC class I antigen. XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; OC Homo. XX RN [1] RP 1-2676 RA Joosten I.; RT ; RL Submitted (30-AUG-2007) to the INSDC. RL Joosten I., ABTI 469, University Medical Centre St Radboud, P.O. Box 9101, RL 6500 HB Nijmegen, NETHERLANDS. XX RN [2] RX DOI; 10.1111/j.1399-0039.2009.01239.x. RX PUBMED; 19493239. RA Tijssen H.J., Driessen S.W., van Houwelingen K.P., Allebes W.A., RA Joosten I.; RT "Complete genomic sequence of a novel HLA-B allele, B*4456N"; RL Tissue Antigens 73(6):607-609(2009). XX DR MD5; 9f4096b3d18c680a46474dc861098966. DR IMGT/HLA; HLA-B*44:56N; HLA03130. XX FH Key Location/Qualifiers FH FT source 1..2676 FT /organism="Homo sapiens" FT /chromosome="6" FT /map="6p21.3" FT /lab_host="Escherichia coli TOP10" FT /mol_type="genomic DNA" FT /sex="male" FT /cell_type="leucocyte" FT /tissue_type="peripheral blood" FT /db_xref="taxon:9606" FT CDS join(1..73,203..472,716..741) FT /gene="HLA-B" FT /allele="HLA-B*44new" FT /product="MHC class I antigen" FT /function="antigen presenting molecule" FT /db_xref="InterPro:IPR001039" FT /db_xref="InterPro:IPR011161" FT /db_xref="InterPro:IPR011162" FT /db_xref="InterPro:IPR037055" FT /db_xref="UniProtKB/TrEMBL:A8KNJ4" FT /protein_id="CAO98865.1" FT /translation="MRVTAPRTLLLLLWGAVALTETWAGSHSMRYFYTAMSRPGRGEPR FT FITVGYVDDTLFVRFDSDATSPRKEPRAPWIEQEGPEYWDRETQISKTNTQTYRENLRT FT ALRYYNQSEAGSHIIQRM" FT exon 1..73 FT /gene="HLA-B" FT /allele="HLA-B*44new" FT /number=1 FT intron 74..202 FT /gene="HLA-B" FT /allele="HLA-B*44new" FT /number=1 FT exon 203..472 FT /gene="HLA-B" FT /allele="HLA-B*44new" FT /number=2 FT intron 473..715 FT /gene="HLA-B" FT /allele="HLA-B*44new" FT /number=2 FT exon 716..741 FT /gene="HLA-B" FT /allele="HLA-B*44new" FT /number=3 XX SQ Sequence 2676 BP; 499 A; 795 C; 856 G; 525 T; 1 other; atgcgggtca cggcgccccg aaccctcctc ctgctgctct ggggggcagt ggccctgacc 60 gagacctggg ccggtgagtg cggggtcggg agggaaatgg cctctgtggg gaggagagag 120 gggaccgcag gcgggggcgc aggacccggg gagccgcgcc gggaggaggg tcgggcgggt 180 ctcagcccct cctcgccccc aggctcccac tccatgaggt atttctacac cgccatgtcc 240 cggcccggcc gcggggagcc ccgcttcatc accgtgggct acgtggacga cacgctgttc 300 gtgaggttcg acagcgacgc cacgagtccg aggaaggagc cgcgggcgcc atggatagag 360 caggaggggc cggagtattg ggaccgggag acacagatct ccaagaccaa cacacagact 420 taccgagaga acctgcgcac cgcgctccgc tactacaacc agagcgaggc cggtgagtga 480 ccccggcccg gggcgcaggt cacgactccc catcccccac gtacggcccg ggtcgccccg 540 agtctccggg tccgagatcc gcccccgagg ccgcgggacc cgcccagacc ctcgaccggc 600 gagagcccca ggcgcgttta cccggtttca ttttcagttg aggccaaaat ccccgcgggt 660 tggtcggggc ggggcggggc tcgggggacg gggctgaccg cggggccggg gccagggtct 720 cacatcatcc agaggatgta aggctgcgac gtggggccgg acgggcgcct cctccgcggg 780 tatgaccagg acgcctacga cggcaaggat tacatcgccc tgaacgagga cctgagctcc 840 tggaccgcgg cggacaccgc ggctcagatc acccagcgca agtgggaggc ggcccgtgtg 900 gcggagcagc ggagagccta cctggagggc acgtgcgtgg agtcgctccg cagatacctg 960 gagaacggga aggagacgct gcagcgcgcg ggtaccaggg gcagtgggga gccttcccca 1020 tctcctatag gtcgccgggg atggcctccc acgagaagag gaggaaaatg ggatcagcgc 1080 tagaatgtcg ccctcccttg aatggagaat ggcatgagtt ttcctgagtt tcctctgagg 1140 gccccctctt ctctctagga caattaaggg atgacgtctc tgaggaaatg gaggggaaga 1200 cagtccctag aatactgatc aggggtcccc tttgacccct gcagcagcct tgggaaccgt 1260 gacttttcct ctcaggcctt gttctctgcc tcacactcag tgtgtttggg gctctgattc 1320 cagcacttct gagtcacttt acctccactc agatcaggag cagaagtccc tgttccccgc 1380 tcagagactc gaactttcca atgaatagga gattatccca ggtgcctgcg tccaggctgg 1440 tgtctggntt ctgtgcccct tccccacccc aggtgtcctg tccattctca ggctggtcac 1500 atgggtggtc ctagggtgtc ccatgagaga tgcaaagcgc ctgaattttc tgactcttcc 1560 catcagaccc cccaaagaca catgtgaccc accaccccat ctctgaccat gaggtcaccc 1620 tgaggtgctg ggccctgggc ttctaccctg cggagatcac actgacctgg cagcgggatg 1680 gcgaggacca aactcaggac accgagcttg tggagaccag accagcagga gatagaacct 1740 tccagaagtg ggcagctgtg gtggtgcctt ctggagaaga gcagagatac acatgccatg 1800 tacagcatga ggggctgccg aagcccctca ccctgagatg gggtaaggag ggggatgagg 1860 ggtcatatct cttctcaggg aaagcaggag cccttcagca gggtcagggc ccctcatctt 1920 cccttccttt cccagagccg tcttcccagt ccaccgtccc catcgtgggc attgttgctg 1980 gcctggctgt cctagcagtt gtggtcatcg gagctgtggt cgctgctgtg atgtgtagga 2040 ggaagagctc aggtagggaa ggggtgaggg gtggggtctg ggttttcttg tcccactggg 2100 ggtttcaagc cccaggtaga agtgttccct gcctcattac tgggaagcag catccacaca 2160 ggggctaacg cagcctggga ccctgtgtgc cagcacttac tcttttgtgc agcacatgtg 2220 acaatgaagg acggatgtat caccttggtg gttgtggcgt tggggtcctg attccagcat 2280 tcatgagtca ggggaaggtc cctgctaagg acagacctta ggagggcagt tggtccagga 2340 cccacacttg ctttcctcgt gtttcctgat cctgccttgg gtctgtagtc atacttctgg 2400 aaattccttt tgggtccaag acgaggaggt tcctctaaga tctcatggcc ctgcttcctc 2460 ccagtcccct cacagggcat tttcttccca caggtggaaa aggagggagc tactctcagg 2520 ctgcgtgtaa gtgatggggg cgggagtgtg gaggagctca cccaccccat aattcctcct 2580 gtcccacgtc tcctgcgggc tctgaccagg tcctgttttt gttctactcc aggcagcgac 2640 agtgcccagg gctctgatgt gtctctcaca gcttga 2676 //