ID U90558; SV 1; linear; genomic DNA; STD; HUM; 949 BP.
XX
AC U90558;
XX
DT 17-NOV-1999 (Rel. 61, Created)
DT 17-JUN-2008 (Rel. 96, Last updated, Version 4)
XX
DE Homo sapiens MHC class I antigen HLA-B heavy chain (HLA-B*1402 allele)
DE gene, partial cds.
XX
KW .
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 1-949
RX DOI; 10.1034/j.1399-0039.1999.530205.x.
RX PUBMED; 10090615.
RA Gomez-Casado E., Vargas-Alarcon G., Martinez-Laso J., Granados J.,
RA Varela P., Alegre R., Longas J., Gonzalez-Hevilla M., Martin-Villa J.M.,
RA Arnaiz-Villena A.;
RT "Evolutionary relationships between HLA-B alleles as indicated by an
RT analysis of intron sequences";
RL Tissue Antigens 53(2):153-160(1999).
XX
RN [2]
RP 1-949
RA Arnaiz-Villena A.;
RT ;
RL Submitted (25-FEB-1997) to the INSDC.
RL Inmunologia, Hospital 12 De Octubre, Carretera De Andalucia, Madrid 28041,
RL Spain
XX
DR MD5; ea000a8758cc3b44467420f0022a0785.
XX
FH Key Location/Qualifiers
FH
FT source 1..949
FT /organism="Homo sapiens"
FT /chromosome="6"
FT /mol_type="genomic DNA"
FT /cell_type="leukocyte"
FT /tissue_type="blood"
FT /db_xref="taxon:9606"
FT mRNA join(<1..29,158..427,674..>949)
FT /gene="HLA-B"
FT /product="MHC class I antigen HLA-B heavy chain"
FT exon <1..29
FT /gene="HLA-B"
FT /number=1
FT CDS join(<1..29,158..427,674..>949)
FT /codon_start=2
FT /gene="HLA-B"
FT /product="MHC class I antigen HLA-B heavy chain"
FT /note="Allele: B*1402; HLA class I heavy chain"
FT /db_xref="IMGT/HLA:B*14:02:01"
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:Q9TP48"
FT /protein_id="AAF08604.1"
FT /translation="ALALTETWAGSHSMRYFYTAVSRPGRGEPRFISVGYVDDTQFVRF
FT DSDAASPREEPRAPWIEQEGPEYWDRNTQICKTNTQTDRESLRNLRGYYNQSEAGSHTL
FT QWMYGCDVGPDGRLLRGYNQFAYDGKDYIALNEDLSSWTAADTAAQITQRKWEAAREAE
FT QLRAYLEGTCVEWLRRHLENGKETLQRA"
FT intron 30..157
FT /gene="HLA-B"
FT /number=1
FT exon 158..427
FT /gene="HLA-B"
FT /number=2
FT intron 428..673
FT /gene="HLA-B"
FT /number=2
FT exon 674..>949
FT /gene="HLA-B"
FT /number=3
XX
SQ Sequence 949 BP; 164 A; 308 C; 359 G; 118 T; 0 other;
ggccctggcc ctgaccgaga cctgggccgg tgagtgcggg tcgggaggga aatggcctct 60
gccgggagga gcgaggggac cgcaggcggg ggcgcaggac ctgaggagcc gcgccgggag 120
gagggtcggg cgggtttcag cccctcctcg cccccaggct cccactccat gaggtatttc 180
tacaccgccg tgtcccggcc cggccgcggg gagccccgct tcatctcagt gggctacgtg 240
gacgacacgc agttcgtgag gttcgacagc gacgccgcga gtccgagaga ggagccgcgg 300
gcgccgtgga tagagcagga ggggccggaa tattgggacc ggaacacaca gatctgcaag 360
accaacacac agactgaccg agagagcctg cggaacctgc gcggctacta caaccagagc 420
gaggccggtg agtgaccccg gcccggggcg caggtcacga ctccccatcc cccacggacg 480
gcccgggtcg ccccgagtct ccgggtccga gatccgcctc cctgaggccg cgggacccgc 540
ccagaccctc gaccggcgag agccccaggc gcgtttaccc ggtttcattt tcagttgagg 600
ccaaaatccc cgcgggttgg gcggggcggg gcggggctcg gggggactgg gctgaccgcg 660
ggggcggggc cagggtctca caccctccag tggatgtatg gctgcgacgt ggggccggac 720
gggcgcctcc tccgcgggta taaccagttc gcctacgacg gcaaggatta catcgccctg 780
aacgaggacc tgagctcctg gaccgcggcg gacaccgcgg ctcagatcac ccagcgcaag 840
tgggaggcgg cccgtgaggc ggagcagctg agagcctacc tggagggcac gtgcgtggag 900
tggctccgca gacacctgga gaacgggaag gagacgctgc agcgcgcgg 949
//
