Dbfetch
ID EU272660; SV 1; linear; genomic DNA; STD; HUM; 1898 BP. XX AC EU272660; XX DT 30-NOV-2010 (Rel. 107, Created) DT 01-DEC-2010 (Rel. 107, Last updated, Version 2) XX DE Homo sapiens isolate r3 KIR3DL2 (KIR3DL2) gene, KIR3DL2*024 allele, exons 3 DE through 9 and 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[1] RP 1-1898 RA Norman P.J., Gendzekhadze K., Meenagh A., Middleton D., Parham P.; RT "KIR3DL2 is polymorphic 2"; RL Unpublished. XX RN [2] RP 1-1898 RA Norman P.J., Gendzekhadze K., Meenagh A., Middleton D., Parham P.; RT ; RL Submitted (08-NOV-2007) to the INSDC. RL Structural Biology, Stanford University School of Medicine, 299 Campus RL Drive West, Stanford, CA 94305, USA XX DR MD5; 6333abfd179b57a150fa164597de4c97. DR IPD-KIR; KIR3DL2*024; KIR00281. XX FH Key Location/Qualifiers FH FT source 1..1898 FT /organism="Homo sapiens" FT /isolate="r3" FT /mol_type="genomic DNA" FT /note="acronym: KIR3DL2*024" FT /db_xref="taxon:9606" FT gene <1..>1898 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT mRNA join(<1..285,386..685,786..1079,1180..1230,1331..1435, FT 1536..1588,1689..>1898) FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /product="KIR3DL2" FT CDS join(<1..285,386..685,786..1079,1180..1230,1331..1435, FT 1536..1588,1689..1898) FT /codon_start=3 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /product="KIR3DL2" FT /db_xref="GOA:E4W3V8" FT /db_xref="InterPro:IPR003599" FT /db_xref="InterPro:IPR013151" FT /db_xref="InterPro:IPR013783" FT /db_xref="InterPro:IPR036179" FT /db_xref="UniProtKB/TrEMBL:E4W3V8" FT /protein_id="ABZ02166.1" FT /translation="GQDKPFLSAWPSTVVPRGGHVALQCHYRRGFNNFMLYKEDRSHVP FT IFHGRIFQESFIMGPVTPAHAGTYRCRGSRPHSLTGWSAPSNPLVIMVTGNHRKPSLLA FT HPGPLLKSGETVILQCWSDVMFEHFFLHREGISEDPSRLVGQIHDGVSKANFSIGPLMP FT VLAGTYRCYGSVPHSPYQLSAPSDPLDIVITGLYEKPSLSAQPGPTVQAGENVTLSCSS FT WSSYDIYHLSREGEAHERRLRAVPKVNRTFQADFPLGPATHGGTYRCFGSFRALPCVWS FT NSSDPLLVSVTGNPSSSWPSPTEPSSKSGICRHLHVLIGTSVVIFLFILLLFFLLYRWC FT SNKKNAAVMDQEPAGDRTVNRQDSDEQDPQEVMYAQLDHCVFIQRKISRPSQRPKTPLT FT DTSVYTELPNAEPRSKVVSCPRAPQSGLEGVF" FT exon 1..285 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /number=3 FT gap 286..385 FT /estimated_length=unknown FT exon 386..685 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /number=4 FT gap 686..785 FT /estimated_length=unknown FT exon 786..1079 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /number=5 FT gap 1080..1179 FT /estimated_length=unknown FT exon 1180..1230 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /number=6 FT gap 1231..1330 FT /estimated_length=unknown FT exon 1331..1435 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /number=7 FT gap 1436..1535 FT /estimated_length=unknown FT exon 1536..1588 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /number=8 FT gap 1589..1688 FT /estimated_length=unknown FT exon 1689..1898 FT /gene="KIR3DL2" FT /allele="KIR3DL2*024" FT /number=9 XX SQ Sequence 1898 BP; 294 A; 396 C; 311 G; 297 T; 600 other; gtggtcagga caaacccttc ctgtctgcct ggcccagcac tgtggtgcct cgaggaggac 60 acgtggctct tcagtgtcac tatcgtcgtg ggtttaacaa tttcatgctg tacaaagaag 120 acagaagcca cgttcccatc ttccacggca gaatattcca ggagagcttc atcatgggcc 180 ctgtgacccc agcacatgca gggacctaca gatgtcgggg ttcacgccca cactccctca 240 ctgggtggtc ggcacccagc aaccccctgg tgatcatggt cacagnnnnn nnnnnnnnnn 300 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 360 nnnnnnnnnn nnnnnnnnnn nnnnngaaac cacagaaaac cttccctcct ggcccaccca 420 gggcccctgc tgaaatcagg agagacagtc atcctgcaat gttggtcaga tgtcatgttt 480 gagcacttct ttctgcacag agaggggatc tctgaggacc cctcacgcct cgttggacag 540 atccatgatg gggtctccaa ggccaacttc tccatcggtc ccttgatgcc tgtccttgca 600 ggaacctaca gatgttatgg ttctgttcct cactccccct atcagttgtc agctcccagt 660 gaccccctgg acatcgtgat cacagnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 720 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 780 nnnnngtcta tatgagaaac cttctctctc agcccagccg ggccccacgg ttcaggcagg 840 agagaacgtg accttgtcct gtagctcctg gagctcctat gacatctacc atctgtccag 900 ggaaggggag gcccatgaac gtaggctccg tgcagtgccc aaggtcaaca gaacattcca 960 ggcagacttt cctctgggcc ctgccaccca cggagggacc tacagatgct tcggctcttt 1020 ccgtgccctg ccctgcgtgt ggtcaaactc aagtgaccca ctgcttgttt ctgtcacagn 1080 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 1140 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnng aaacccttca agtagttggc 1200 cttcacccac agaaccaagc tccaaatctg nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 1260 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 1320 nnnnnnnnnn gtatctgcag acacctgcat gttctgattg ggacctcagt ggtcatcttc 1380 ctcttcatcc tcctcctctt ctttctcctt tatcgctggt gctccaacaa aaagannnnn 1440 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 1500 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnatgct gctgtaatgg accaagagcc 1560 tgcgggggac agaacagtga ataggcagnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 1620 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 1680 nnnnnnnnga ctctgatgaa caagaccctc aggaggtgat gtacgcacag ttggatcact 1740 gcgttttcat acagagaaaa atcagtcgcc cttctcagag gcccaagaca cccctaacag 1800 ataccagcgt gtacacggaa cttccaaatg ctgagcccag atccaaagtt gtctcctgcc 1860 cacgagcacc acagtcaggt cttgaggggg ttttctag 1898 //