Dbfetch

ID   LT599263; SV 1; linear; genomic DNA; STD; HUM; 3334 BP.
XX
AC   LT599263;
XX
DT   14-JUL-2016 (Rel. 129, Created)
DT   19-JUL-2017 (Rel. 133, Last updated, Version 3)
XX
DE   Homo sapiens, HLA-B gene for MHC class I antigen, cell line
DE   DKMS-LSL-B-1201, allele HLA-B*44:new
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   1-3334
RA   Albrecht V.;
RT   ;
RL   Submitted (06-JUN-2016) to the INSDC.
RL   Research and Development, DKMS Life Science Lab, Fiedler Str. 43, Saxony,
RL   01307 Dresden, GERMANY.
XX
RN   [2]
RX   DOI; https://doi.org/10.1111/tan.13057.
RX   PUBMED; 28547825.
RA   Albrecht V., Zweiniger C., Surendranath V., Lang K., Schofl G., Dahl A.,
RA   Winkler S., Lange V., Bohme I., Schmidt A.H.;
RT   "Dual redundant sequencing strategy: Full-length gene characterisation of
RT   1056 novel and confirmatory HLA alleles";
RL   HLA. -:1-9(2017).
XX
DR   MD5; 4e1ddfa709858f23a02f9a0f35793215.
DR   IMGT/HLA; HLA-B*44:27:01:01; HLA01489.
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..3334
FT                   /organism="Homo sapiens"
FT                   /mol_type="genomic DNA"
FT                   /cell_line="DKMS-LSL-B-1201"
FT                   /db_xref="taxon:9606"
FT   exon            1..357
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=1
FT   CDS             join(285..357,487..756,1000..1275,1851..2126,2231..2347,
FT                   2789..2821,2928..2971)
FT                   /codon_start=1
FT                   /transl_table=1
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /product="MHC class I antigen"
FT                   /function="antigen presenting molecule"
FT                   /db_xref="GOA:A0A0B7MH47"
FT                   /db_xref="InterPro:IPR001039"
FT                   /db_xref="InterPro:IPR003006"
FT                   /db_xref="InterPro:IPR003597"
FT                   /db_xref="InterPro:IPR007110"
FT                   /db_xref="InterPro:IPR010579"
FT                   /db_xref="InterPro:IPR011161"
FT                   /db_xref="InterPro:IPR011162"
FT                   /db_xref="InterPro:IPR013783"
FT                   /db_xref="InterPro:IPR036179"
FT                   /db_xref="InterPro:IPR037055"
FT                   /db_xref="UniProtKB/TrEMBL:A0A0B7MH47"
FT                   /protein_id="SBW38484.1"
FT                   /translation="MRVTAPRTLLLLLWGAVALTETWAGSHSMRYFYTAMSRPGRGEPR
FT                   FITVGYVDDTLFVRFDSDATSPRKEPRAPWIEQEGPEYWDRETQISKTNTQTYRENLRT
FT                   ALRYYNQSEAGSHIIQRMYGCDVGPDGRLLRGYDQDAYDGKDYIALNEDLSSWTAADTA
FT                   AQITQRKWEAARVAEQDRAYLEGLCVESLRRYLENGKETLQRADPPKTHVTHHPISDHE
FT                   ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDRTFQKWAAVVVPSGEEQRY
FT                   TCHVQHEGLPKPLTLRWEPSSQSTIPIVGIVAGLAVLAVVVIGAVVATVMCRRKSSGGK
FT                   GGSYSQAASSDSAQGSDVSLTA"
FT   intron          358..486
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=1
FT   exon            487..756
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=2
FT   intron          757..999
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=2
FT   exon            1000..1275
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=3
FT   intron          1276..1850
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=3
FT   exon            1851..2126
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=4
FT   intron          2127..2230
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=4
FT   exon            2231..2347
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=5
FT   intron          2348..2788
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=5
FT   exon            2789..2821
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=6
FT   intron          2822..2927
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=6
FT   exon            2928..3334
FT                   /gene="HLA-B"
FT                   /allele="HLA-B*44:new"
FT                   /number=7
XX
SQ   Sequence 3334 BP; 619 A; 970 C; 1050 G; 695 T; 0 other;
     gatcaggacg aagtcccagg tcccggacgg ggctctcagg gtctcaggct ccgagggccg        60
     cgtctgcaat ggggaggcgc agcgttgggg attccccact cccacgagtt tcacttcttc       120
     tcccaaccta tgtcgggtcc ttcttccagg atactcgtga cgcgtcccca tttcccactc       180
     ccattgggtg tcgggtgtct agagaagcca atcagtgtcg ccggggtccc agttctaaag       240
     tccccacgca cccacccgga ctcagaatct cctcagacgc cgagatgcgg gtcacggcgc       300
     cccgaaccct cctcctgctg ctctgggggg cagtggccct gaccgagacc tgggccggtg       360
     agtgcggggt cgggagggaa atggcctctg tggggaggag agaggggacc gcaggcgggg       420
     gcgcaggacc cggggagccg cgccgggagg agggtcgggc gggtctcagc ccctcctcgc       480
     ccccaggctc ccactccatg aggtatttct acaccgccat gtcccggccc ggccgcgggg       540
     agccccgctt catcaccgtg ggctacgtgg acgacacgct gttcgtgagg ttcgacagcg       600
     acgccacgag tccgaggaag gagccgcggg cgccatggat agagcaggag gggccggagt       660
     attgggaccg ggagacacag atctccaaga ccaacacaca gacttaccga gagaacctgc       720
     gcaccgcgct ccgctactac aaccagagcg aggccggtga gtgaccccgg cccggggcgc       780
     aggtcacgac tccccatccc ccacgtacgg cccgggtcgc cccgagtctc cgggtccgag       840
     atccgccccc gaggccgcgg gacccgccca gaccctcgac cggcgagagc cccaggcgcg       900
     tttacccggt ttcattttca gttgaggcca aaatccccgc gggttggtcg gggcggggcg       960
     gggctcgggg gacggggctg accgcggggc cggggccagg gtctcacatc atccagagga      1020
     tgtacggctg cgacgtgggg ccggacgggc gcctcctccg cgggtatgac caggacgcct      1080
     acgacggcaa ggattacatc gccctgaacg aggacctgag ctcctggacc gcggcggaca      1140
     ccgcggctca gatcacccag cgcaagtggg aggcggcccg tgtggcggag caggacagag      1200
     cctacctgga gggcctgtgc gtggagtcgc tccgcagata cctggagaac gggaaggaga      1260
     cgctgcagcg cgcgggtacc aggggcagtg gggagccttc cccatctcct ataggtcgcc      1320
     ggggatggcc tcccacgaga agaggaggaa aatgggatca gcgctagaat gtcgccctcc      1380
     cttgaatgga gaatggcatg agttttcctg agtttcctct gagggccccc tcttctctct      1440
     aggacaatta agggatgacg tctctgagga aatggagggg aagacagtcc ctagaatact      1500
     gatcaggggt cccctttgac ccctgcagca gccttgggaa ccgtgacttt tcctctcagg      1560
     ccttgttctc tgcctcacac tcagtgtgtt tggggctctg attccagcac ttctgagtca      1620
     ctttacctcc actcagatca ggagcagaag tccctgttcc ccgctcagag actcgaactt      1680
     tccaatgaat aggagattat cccaggtgcc tgcgtccagg ctggtgtctg ggttctgtgc      1740
     cccttcccca ccccaggtgt cctgtccatt ctcaggctgg tcacatgggt ggtcctaggg      1800
     tgtcccatga gagatgcaaa gcgcctgaat tttctgactc ttcccatcag accccccaaa      1860
     gacacatgtg acccaccacc ccatctctga ccatgaggcc accctgaggt gctgggccct      1920
     gggcttctac cctgcggaga tcacactgac ctggcagcgg gatggcgagg accaaactca      1980
     ggacaccgag cttgtggaga ccagaccagc aggagataga accttccaga agtgggcagc      2040
     tgtggtggtg ccttctggag aagagcagag atacacatgc catgtacagc atgaggggct      2100
     gccgaagccc ctcaccctga gatggggtaa ggagggggat gaggggtcat atctgttctc      2160
     agggaaagca ggagcccttc tggagccctt cagcagggtc agggcccctc atcttcccct      2220
     cctttcccag agccatcttc ccagtccacc atccccatcg tgggcattgt tgctggcctg      2280
     gctgtcctag cagttgtggt catcggagct gtggtcgcta ctgtgatgtg taggaggaag      2340
     agctcaggta gggaaggggt gaggggtggg gtctgggttt tcttgtccca ctgggggttt      2400
     caagccccag gtagaagtgt tccctgcctc attactggga agcagcatcc acacaggggc      2460
     taacgcagcc tgggaccctg tgtgccagca cttactcttt tgtgcagcac atgtgacaat      2520
     gaaggacaga tgtatcgcct tgatggttgt ggtgttgggg tcctgattcc agcattcatg      2580
     agtcagggga aggtccctgc taaggacaga ccttaggagg gcagttggtc caggacccac      2640
     acttgctttc ctcgtgtttc ctgatcctgc cctgggtctg tagtcatact tctggaaatt      2700
     ccttttggtt ccaagacgag gaggttcctc taagatctca tggtcctgct tcctcccagt      2760
     cccctcacag gacattttct tcccacaggt ggaaaaggag ggagctactc tcaggctgcg      2820
     tgtaagtggt gggggtggga gtgtggagga gctcacccac cccataattc ctcctgtccc      2880
     acgtctcctg cgggctctga ccaggtcctg tttttgttct actccagcca gcgacagtgc      2940
     ccagggctct gatgtgtctc tcacagcttg aaaaggtgag attcttgggg tctagagtgg      3000
     gtggggtggc gggtctgggg gtgggtgggg cagtggggaa aggcctgggt aatggagatt      3060
     ctttgattgg gatgtttcgc gtgtgtcgtg ggctgttcag agtgtcatca cttaccatga      3120
     ctaaccagaa tttgttcatg actgttgttt tctgtagcct gagacagctg tcttgtgagg      3180
     gactgagatg caggatttct tcacgcctcc cctttgtgac ttcaagagcc tctggcatct      3240
     ctttctgcaa aggcacctga atgtgtctgc gtccctgtta gcataatgtg aggaggtgga      3300
     gagacagccc acccttgtgt ccactgtgac ccct                                  3334
//