Dbfetch
ID L42296; SV 1; linear; genomic DNA; STD; HUM; 774 BP.
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AC L42296;
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DT 24-JAN-1996 (Rel. 46, Created)
DT 17-JUN-2008 (Rel. 96, Last updated, Version 6)
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DE Homo sapiens MHC HLA-B*1501 gene, exons 2 and 3.
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KW cell surface antigen; cell surface glycoprotein; class I gene; HLA-B*1501;
KW integral membrane protein; major histocompatibility complex.
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OS Homo sapiens (human)
OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC Homo.
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RN [1]
RP 1-774
RX DOI; 10.1016/S0198-8859(97)00090-6.
RX PUBMED; 9361971.
RA Wang J., Fernandez-Vina M.A., Lazaro A.M., Shumway W., LeFor W.,
RA Stastny P.;
RT "New alleles of the HLA-B15 family";
RL Hum. Immunol. 55(2):184-189(1997).
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DR MD5; 58355b2e4b6734eaa686e712905ac1bb.
DR IMGT/HLA; HLA-B*15:30:01:01; HLA00193.
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FH Key Location/Qualifiers
FH
FT source 1..774
FT /organism="Homo sapiens"
FT /mol_type="genomic DNA"
FT /cell_type="leukocytes"
FT /db_xref="taxon:9606"
FT exon <1..257
FT /gene="HLA-B*1501"
FT /number=2
FT intron 258..502
FT /gene="HLA-B*1501"
FT /number=2
FT exon 503..>774
FT /gene="HLA-B*1501"
FT /number=3
FT variation 571
FT /gene="HLA-B*1501"
FT /replace="a"
FT variation 578
FT /gene="HLA-B*1501"
FT /replace="a"
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SQ Sequence 774 BP; 141 A; 255 C; 278 G; 100 T; 0 other;
gaggtatttc tacaccgcca tgtcccggcc cggccgcggg gagccccgct tcatcgcagt 60
gggctacgtg gacgacaccc agttcgtgag gttcgacagc gacgccgcga gtccgaggat 120
ggcgccccgg gcgccatgga tagagcagga ggggccggag tattgggacc gggagacaca 180
gatctccaag accaacacac agacttaccg agagagcctg cggaacctgc gcggctacta 240
caaccagagc gaggccggtg agtgaccccg gcctggggcg caggtcacga ctccccatcc 300
cccacgtacg gcccgggtcg ccccgagtct ccgggtccga gatccgcccc cctgaggccg 360
cgggacccgc ccaaaccctc gaccggcgag agccccaggc gcgtttaccc ggtttcattt 420
tcagttgagg ccaaaatccc cgcgggttgg tcggggcggg gcggggctcg ggggacgggg 480
ctgaccgcgg ggcctgggcc agggtctcac accctccaga ggatgtacgg ctgcgacgtg 540
gggccggacg ggcgcctcct ccgcgggcat aaccagtacg cctacgacgg caaggattac 600
atcgccctga acgaggacct gagctcctgg accgcggcgg acacggcggc tcagatcacc 660
cagcgcaagt gggaggcggc ccgtgaggcg gagcagtgga gagcctacct ggagggcctg 720
tgcgtggagt ggctccgcag atacctggag aacgggaagg agacgctgca gcgc 774
//