2024-03-29 08:53:38, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_197974 2927 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens butyrophilin, subfamily 3, member A3 (BTN3A3), transcript variant 2, mRNA. ACCESSION NM_197974 VERSION NM_197974.2 GI:261490683 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. REFERENCE 1 (bases 1 to 2927) AUTHORS Smith,I.A., Knezevic,B.R., Ammann,J.U., Rhodes,D.A., Aw,D., Palmer,D.B., Mather,I.H. and Trowsdale,J. TITLE BTN1A1, the mammary gland butyrophilin, and BTN2A2 are both inhibitors of T cell activation JOURNAL J. Immunol. 184 (7), 3514-3525 (2010) PUBMED 20208008 REFERENCE 2 (bases 1 to 2927) AUTHORS Zhang,Z. and Henzel,W.J. TITLE Signal peptide prediction based on analysis of experimentally verified cleavage sites JOURNAL Protein Sci. 13 (10), 2819-2824 (2004) PUBMED 15340161 REFERENCE 3 (bases 1 to 2927) AUTHORS Rhodes,D.A., Stammers,M., Malcherek,G., Beck,S. and Trowsdale,J. TITLE The cluster of BTN genes in the extended major histocompatibility complex JOURNAL Genomics 71 (3), 351-362 (2001) PUBMED 11170752 REFERENCE 4 (bases 1 to 2927) AUTHORS Henry,J., Miller,M.M. and Pontarotti,P. TITLE Structure and evolution of the extended B7 family JOURNAL Immunol. Today 20 (6), 285-288 (1999) PUBMED 10354554 REMARK Review article REFERENCE 5 (bases 1 to 2927) AUTHORS Ruddy,D.A., Kronmal,G.S., Lee,V.K., Mintier,G.A., Quintana,L., Domingo,R. Jr., Meyer,N.C., Irrinki,A., McClelland,E.E., Fullan,A., Mapa,F.A., Moore,T., Thomas,W., Loeb,D.B., Harmon,C., Tsuchihashi,Z., Wolff,R.K., Schatzman,R.C. and Feder,J.N. TITLE A 1.1-Mb transcript map of the hereditary hemochromatosis locus JOURNAL Genome Res. 7 (5), 441-456 (1997) PUBMED 9149941 COMMENT VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from DC410234.1, AK301553.1 and BC015815.2. On Oct 17, 2009 this sequence version replaced gi:37574627. Summary: The butyrophilin (BTN) genes are a group of major histocompatibility complex (MHC)-associated genes that encode type I membrane proteins with 2 extracellular immunoglobulin (Ig) domains and an intracellular B30.2 (PRYSPRY) domain. Three subfamilies of human BTN genes are located in the MHC class I region: the single-copy BTN1A1 gene (MIM 601610) and the BTN2 (e.g., BTN2A1; MIM 613590) and BTN3 (e.g., BNT3A3) genes, which have undergone tandem duplication, resulting in 3 copies of each (summary by Smith et al., 2010 [PubMed 20208008]).[supplied by OMIM, Nov 2010]. Transcript Variant: This variant (2) differs in the 5' UTR, lacks a portion of the 5' coding region, uses a downstream translational start codon, and lacks an alternate in-frame exon in the central coding region, compared to variant 1. The encoded isoform (b) is shorter than isoform a. ##Evidence-Data-START## Transcript exon combination :: AK301553.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025088 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-16 DC410234.1 1-16 17-857 AK301553.1 1-841 858-883 BC015815.2 866-891 884-2144 AK301553.1 868-2128 2145-2927 BC015815.2 2174-2956 FEATURES Location/Qualifiers source 1..2927 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="6" /map="6p21.3" gene 1..2927 /gene="BTN3A3" /gene_synonym="BTF3" /note="butyrophilin, subfamily 3, member A3" /db_xref="GeneID:10384" /db_xref="HGNC:1140" /db_xref="MIM:613595" exon 1..177 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 93 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:114195506" variation 121 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:117832370" misc_feature 152..154 /gene="BTN3A3" /gene_synonym="BTF3" /note="upstream in-frame stop codon" exon 178..238 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 182 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:7751645" variation 220 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:370604128" exon 239..257 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" exon 258..605 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 282 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:375578358" CDS 299..1906 /gene="BTN3A3" /gene_synonym="BTF3" /note="isoform b is encoded by transcript variant 2; butyrophilin 3" /codon_start=1 /product="butyrophilin subfamily 3 member A3 isoform b" /protein_id="NP_932078.2" /db_xref="GI:261490684" /db_xref="CCDS:CCDS4612.2" /db_xref="GeneID:10384" /db_xref="HGNC:1140" /db_xref="MIM:613595" /translation="
MVGEDADLPCHLFPTMSAETMELRWVSSSLRQVVNVYADGKEVEDRQSAPYRGRTSILRDGITAGKAALRIHNVTASDSGKYLCYFQDGDFYEKALVELKVAALGSDLHIEVKGYEDGGIHLECRSTGWYPQPQIKWSDTKGENIPAVEAPVVADGVGLYAVAASVIMRGSSGGGVSCIIRNSLLGLEKTASISIADPFFRSAQPWIAALAGTLPISLLLLAGASYFLWRQQKEKIALSRETEREREMKEMGYAATEQEISLREWRKIQYMARGEKSLAYHEWKMALFKPADVILDPDTANAILLVSEDQRSVQRAEEPRDLPDNPERFEWRYCVLGCENFTSGRHYWEVEVGDRKEWHIGVCSKNVERKKGWVKMTPENGYWTMGLTDGNKYRALTEPRTNLKLPEPPRKVGIFLDYETGEISFYNATDGSHIYTFPHASFSEPLYPVFRILTLEPTALTICPIPKEVESSPDPDLVPDHSLETPLTPGLANESGEPQAEVTSLLLPAHPGAEVSPSATTNQNHKLQARTEALY
" misc_feature 305..604 /gene="BTN3A3" /gene_synonym="BTF3" /note="Immunoglobulin (Ig)-like domain of myelin oligodendrocyte glycoprotein (MOG); Region: Ig_MOG_like; cd05713" /db_xref="CDD:143190" misc_feature 311..550 /gene="BTN3A3" /gene_synonym="BTF3" /note="Immunoglobulin V-Type; Region: IGv; smart00406" /db_xref="CDD:197704" misc_feature order(353..358,413..415,446..448,557..559,563..580) /gene="BTN3A3" /gene_synonym="BTF3" /note="antigen binding site; other site" /db_xref="CDD:143190" misc_feature 1166..1321 /gene="BTN3A3" /gene_synonym="BTF3" /note="associated with SPRY domains; Region: PRY; smart00589" /db_xref="CDD:128857" misc_feature 1325..1693 /gene="BTN3A3" /gene_synonym="BTF3" /note="Domain in SPla and the RYanodine Receptor; Region: SPRY; smart00449" /db_xref="CDD:128725" variation 314 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:376102561" variation 339 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:368285328" variation 340 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:77474489" variation 345 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200536472" variation 358 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371864834" variation 376 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201309184" variation 404 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:137957846" variation 431 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:375239049" variation 448 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147078433" variation 452 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:376234984" variation 465 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138755245" variation 473 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:149312684" variation 506 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372313829" exon 606..887 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 630 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:148026276" variation 685 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:138065289" variation 688 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:150636780" variation 695 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:373589611" variation 731 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:374130285" variation 736 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:377686214" variation 740 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201388694" variation 804 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:140844974" variation 810 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:144615747" variation 818 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:147467780" variation 846 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200625612" variation 853 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200139388" variation 874 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:202187130" variation 881 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:139877036" variation 883 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:3846848" exon 888..1088 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 890 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:41266843" variation 904 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:142420060" variation 905 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:151329283" variation 907 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:368341416" variation 921 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:371579409" variation 949 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:368908067" variation 961 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:371725478" variation 987 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:146453476" variation 1035 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:140949337" variation 1047 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200302181" variation 1052 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200631543" variation 1057 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:375083429" variation 1058 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:144686528" variation 1084 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201850379" exon 1089..1115 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1109 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:202118130" variation 1110 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:140111422" variation 1111 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150366659" exon 1116..1142 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1121 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:138105205" variation 1127 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:74640395" variation 1128 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:79652472" exon 1143..1169 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1144 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:201134941" exon 1170..2910 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1171 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200780915" variation 1194 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:199818322" variation 1196 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:112698147" variation 1198 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:368263332" variation 1201 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:201403401" variation 1206 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:370679491" variation 1215 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:374373356" variation 1229 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:149504053" variation 1236 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:114347679" variation 1237 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200995489" variation 1255 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:141739374" variation 1273 /gene="BTN3A3" /gene_synonym="BTF3" /replace="" /replace="c" /db_xref="dbSNP:35279486" variation 1291 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:116318960" variation 1292 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200026955" variation 1293 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147489251" variation 1303 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:139835450" variation 1307 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:367977572" variation 1333 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371833271" variation 1336 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:142830190" variation 1339 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:150687753" variation 1365 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150755364" variation 1370 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:375702813" variation 1413 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:149823309" variation 1414 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:367714257" variation 1430 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:113551647" variation 1431 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:146835625" variation 1432 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:140664333" variation 1437 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:139072503" variation 1447 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:372614651" variation 1459 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:143237800" variation 1476 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:146699487" variation 1478 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:148819206" variation 1486 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:143460142" variation 1503 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:151008942" variation 1516 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:370056298" variation 1519 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:374128957" variation 1535 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:368736832" variation 1538 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:189581403" variation 1541 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:181680390" variation 1552 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:140904550" variation 1562 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:369319317" variation 1564 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:146179367" variation 1569 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138799361" variation 1576 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:142813836" variation 1600 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200849554" variation 1606 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371096421" variation 1616 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147058580" variation 1632 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372897235" variation 1640 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372318760" variation 1656 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138234810" variation 1682 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:376332419" variation 1729 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:369647186" variation 1737 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:372009871" variation 1750 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:375200446" variation 1796 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:369331349" variation 1799 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:372494707" variation 1804 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:149459247" variation 1828 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:201968625" variation 1854 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:79308763" variation 1863 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201113386" variation 1886 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:140210209" variation 1887 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:144256388" variation 1889 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:148720535" variation 1928 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:145699923" variation 1943 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:75997823" variation 2058 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:45622835" variation 2105 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:147740049" variation 2214 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:41267923" variation 2244 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:140968699" variation 2259 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:190991772" variation 2303 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:181403362" variation 2352 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:142399461" variation 2400 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:80165853" variation 2446 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:9393721" variation 2476 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:151275014" variation 2503 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:76504501" variation 2647 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:185627402" variation 2671 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:140483657" variation 2682 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150406471" variation 2747 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:374762838" variation 2752 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:367610347" STS 2762..2888 /gene="BTN3A3" /gene_synonym="BTF3" /standard_name="WI-14381" /db_xref="UniSTS:69485" variation 2802..2803 /gene="BTN3A3" /gene_synonym="BTF3" /replace="" /replace="a" /db_xref="dbSNP:113625452" variation 2858 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:9770" variation 2859 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:141194871" variation 2866 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:189698449" variation 2867 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:144928044" variation 2909 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:41267925" ORIGIN
aatcaaaaaactaattcttccaaaaagagattgttattattcctcacaataaccagatagcctctgctttctttttcctttcttcggaatgagagactcaaccataatagaaagaatggagaactattaaccaccattcttcagtgggctgtgattttcagaggggaatactaagaaatggttttccatactggaacccaaaggtaaagacactcaaggacagacatttttggcagagctgctcactccttgctcagctcagttttctgtgcttggaccctctgggcccatcctggccatggtgggtgaagacgctgatctgccctgtcacctgttcccgaccatgagtgcagagaccatggagctgaggtgggtgagttccagcctaaggcaggtggtgaacgtgtatgcagatggaaaggaagtggaagacaggcagagtgcaccgtatcgagggagaacttcgattctgcgggatggcatcactgcagggaaggctgctctccgaatacacaacgtcacagcctctgacagtggaaagtacttgtgttatttccaagatggtgacttctacgaaaaagccctggtggagctgaaggttgcagcattgggttctgatcttcacattgaagtgaagggttatgaggatggagggatccatctggagtgcaggtccactggctggtacccccaaccccaaataaagtggagcgacaccaagggagagaacatcccggctgtggaagcacctgtggttgcagatggagtgggcctgtatgcagtagcagcatctgtgatcatgagaggcagctctggtgggggtgtatcctgcatcatcagaaattccctcctcggcctggaaaagacagccagcatatccatcgcagaccccttcttcaggagcgcccagccctggatcgcggccctggcagggaccctgcctatctcgttgctgcttctcgcaggagccagttacttcttgtggagacaacagaaggaaaaaattgctctgtccagggagacagaaagagagcgagagatgaaagaaatgggatacgctgcaacagagcaagaaataagcctaagagagtggaggaaaatccagtacatggctcgtggagagaagtctttggcctatcatgaatggaaaatggccctcttcaaacctgcggatgtgattctggatccagacacggcaaacgccatcctccttgtttctgaggaccagaggagtgtgcagcgtgctgaagagccgcgggatctgccagacaaccctgagagatttgaatggcgttactgtgtccttggctgtgaaaacttcacatcagggagacattactgggaggtggaagtgggggacagaaaagagtggcatattggggtatgtagtaagaacgtggagaggaaaaaaggttgggtcaaaatgacaccggagaacggatactggactatgggcctgactgatgggaataagtatcgggctctcactgagcccagaaccaacctgaaacttcctgagcctcctaggaaagtggggatcttcctggactatgagactggagagatctcgttctataatgccacagatggatctcatatctacacctttccgcacgcctctttctctgagcctctatatcctgttttcagaattttgaccttggagcccactgccctgaccatttgcccaataccaaaagaagtagagagttcccccgatcctgacctagtgcctgatcattccctggagacaccactgaccccgggcttagctaatgaaagtggggagcctcaggctgaagtaacatctctgcttctccctgcccaccctggagctgaggtctccccttctgcaacaaccaatcagaaccataagctacaggcacgcactgaagcactttactgatattcattccattattccatatgacagttgttttgagtttcgtaccaccttattgtccccttatacagataaggaaactggggtgcagaaaggtgaattaactttacaaagtagacatgacaagtgaacagcagagctgggatctaaacagcaataactaacattaacagagaatttaaaatgttcttagtgctgtgttataagctttggtggatgtcactcctttaatcctcacaacaccctgtcgggtagtcatattttgcaagtatggaagctgaggcagggcaacatgaagtaacttacataactcatacagtaatttgtgcagttgggagatgttcagccttagtccctggctaattgcctgttcttttccagcctgattttttttcccacaggaagagcccacatgtagccctgaggtttccttcccaggacagctgcagggtagagatcattttaagtgcttgtggagttgacatccctattgactctttcccagctgatatcagagacttagacccagcactccttggattagctctgcagagtgtcttggttgagagaataacctcatagtaccaacatgacatgtgacttggaaagagactagaggccacacttgataaatcatggggcacagatatgttcccacccaacaaatgtgataagtgattgtgcagccagagccagccttccttcaatcaaggtttccaggcagagcaaataccctagagattctctgtgatataggaaatttggatcaaggaagctaaaagaattacagggatgtttttaatcccactatggactcagtctcctggaaataggtctgtccactcctggtcattggtggatgttaaacccatattcctttcaactgctgcctgctagggaaaactgctcctcattatcatcactattattgctcaccactgtatcccctctacttggcaagtggttgtcaagttctagttgttcaataaatgtgttaataatgcttaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:10384 -> Biological process: GO:0002456 [T cell mediated immunity] evidence: IMP GeneID:10384 -> Cellular component: GO:0005886 [plasma membrane] evidence: IDA GeneID:10384 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.