2024-03-28 19:01:39, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_006994 3019 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens butyrophilin, subfamily 3, member A3 (BTN3A3), transcript variant 1, mRNA. ACCESSION NM_006994 VERSION NM_006994.4 GI:261490682 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 3019) 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 3019) 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 3019) 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 3019) 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 3019) 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 and BC015815.2. On Oct 17, 2009 this sequence version replaced gi:37574626. 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 (1) represents the longest transcript and encodes the longest isoform (a). ##Evidence-Data-START## Transcript exon combination :: BC015815.2, U90548.1 [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 1-63 DC410234.1 1-63 64-3019 BC015815.2 1-2956 FEATURES Location/Qualifiers source 1..3019 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="6" /map="6p21.3" gene 1..3019 /gene="BTN3A3" /gene_synonym="BTF3" /note="butyrophilin, subfamily 3, member A3" /db_xref="GeneID:10384" /db_xref="HGNC:1140" /db_xref="HPRD:12548" /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" 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..328 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" misc_feature 241..243 /gene="BTN3A3" /gene_synonym="BTF3" /note="upstream in-frame stop codon" CDS 244..1998 /gene="BTN3A3" /gene_synonym="BTF3" /note="isoform a precursor is encoded by transcript variant 1; butyrophilin 3" /codon_start=1 /product="butyrophilin subfamily 3 member A3 isoform a precursor" /protein_id="NP_008925.1" /db_xref="GI:5901908" /db_xref="CCDS:CCDS4611.1" /db_xref="GeneID:10384" /db_xref="HGNC:1140" /db_xref="HPRD:12548" /db_xref="MIM:613595" /translation="
MKMASSLAFLLLNFHVSLFLVQLLTPCSAQFSVLGPSGPILAMVGEDADLPCHLFPTMSAETMELRWVSSSLRQVVNVYADGKEVEDRQSAPYRGRTSILRDGITAGKAALRIHNVTASDSGKYLCYFQDGDFYEKALVELKVAALGSDLHIEVKGYEDGGIHLECRSTGWYPQPQIKWSDTKGENIPAVEAPVVADGVGLYAVAASVIMRGSSGGGVSCIIRNSLLGLEKTASISIADPFFRSAQPWIAALAGTLPISLLLLAGASYFLWRQQKEKIALSRETEREREMKEMGYAATEQEISLREKLQEELKWRKIQYMARGEKSLAYHEWKMALFKPADVILDPDTANAILLVSEDQRSVQRAEEPRDLPDNPERFEWRYCVLGCENFTSGRHYWEVEVGDRKEWHIGVCSKNVERKKGWVKMTPENGYWTMGLTDGNKYRALTEPRTNLKLPEPPRKVGIFLDYETGEISFYNATDGSHIYTFPHASFSEPLYPVFRILTLEPTALTICPIPKEVESSPDPDLVPDHSLETPLTPGLANESGEPQAEVTSLLLPAHPGAEVSPSATTNQNHKLQARTEALY
" sig_peptide 244..330 /gene="BTN3A3" /gene_synonym="BTF3" /inference="COORDINATES: ab initio prediction:SignalP:4.0" mat_peptide 331..1995 /gene="BTN3A3" /gene_synonym="BTF3" /product="Butyrophilin subfamily 3 member A3" /experiment="experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O00478.1)" misc_feature 331..645 /gene="BTN3A3" /gene_synonym="BTF3" /note="Immunoglobulin V-set domain; Region: V-set; pfam07686" /db_xref="CDD:203725" misc_feature 376..675 /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 order(424..429,484..486,517..519,628..630,634..651) /gene="BTN3A3" /gene_synonym="BTF3" /note="antigen binding site; other site" /db_xref="CDD:143190" misc_feature 988..1050 /gene="BTN3A3" /gene_synonym="BTF3" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (O00478.1); transmembrane region" misc_feature 1258..1413 /gene="BTN3A3" /gene_synonym="BTF3" /note="associated with SPRY domains; Region: PRY; smart00589" /db_xref="CDD:128857" misc_feature 1417..1785 /gene="BTN3A3" /gene_synonym="BTF3" /note="Domain in SPla and the RYanodine Receptor; Region: SPRY; smart00449" /db_xref="CDD:128725" variation 276 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:375127466" variation 294 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:56036950" variation 295 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:377535721" exon 329..676 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 353 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:375578358" variation 385 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:376102561" variation 410 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:368285328" variation 411 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:77474489" variation 416 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200536472" variation 429 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371864834" variation 447 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201309184" variation 475 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:137957846" variation 502 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:375239049" variation 519 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147078433" variation 523 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:376234984" variation 536 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138755245" variation 544 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:149312684" variation 577 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372313829" exon 677..958 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 701 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:148026276" variation 756 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:138065289" variation 759 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:150636780" variation 766 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:373589611" variation 802 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:374130285" variation 807 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:377686214" variation 811 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201388694" variation 875 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:140844974" variation 881 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:144615747" variation 889 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:147467780" variation 917 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200625612" variation 924 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200139388" variation 945 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:202187130" variation 952 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:139877036" variation 954 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:3846848" exon 959..1159 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 961 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:41266843" variation 975 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:142420060" variation 976 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:151329283" variation 978 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:368341416" variation 992 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:371579409" variation 1020 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:368908067" variation 1032 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:371725478" variation 1058 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:146453476" variation 1106 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:140949337" variation 1118 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200302181" variation 1123 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200631543" variation 1128 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:375083429" variation 1129 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:144686528" variation 1155 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201850379" exon 1160..1180 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1168 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:369276339" variation 1177 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138503712" exon 1181..1207 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1201 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:202118130" variation 1202 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:140111422" variation 1203 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150366659" exon 1208..1234 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1213 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:138105205" variation 1219 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:74640395" variation 1220 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:79652472" exon 1235..1261 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1236 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:201134941" exon 1262..3002 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 1263 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200780915" variation 1286 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:199818322" variation 1288 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:112698147" variation 1290 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:368263332" variation 1293 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:201403401" variation 1298 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:370679491" variation 1307 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:374373356" variation 1321 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:149504053" variation 1328 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:114347679" variation 1329 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200995489" variation 1347 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:141739374" variation 1365 /gene="BTN3A3" /gene_synonym="BTF3" /replace="" /replace="c" /db_xref="dbSNP:35279486" variation 1383 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:116318960" variation 1384 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200026955" variation 1385 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147489251" variation 1395 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:139835450" variation 1399 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:367977572" variation 1425 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371833271" variation 1428 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:142830190" variation 1431 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:150687753" variation 1457 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150755364" variation 1462 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:375702813" variation 1505 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:149823309" variation 1506 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:367714257" variation 1522 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:113551647" variation 1523 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:146835625" variation 1524 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:140664333" variation 1529 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:139072503" variation 1539 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:372614651" variation 1551 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:143237800" variation 1568 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:146699487" variation 1570 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:148819206" variation 1578 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:143460142" variation 1595 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:151008942" variation 1608 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:370056298" variation 1611 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:374128957" variation 1627 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:368736832" variation 1630 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:189581403" variation 1633 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:181680390" variation 1644 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:140904550" variation 1654 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:369319317" variation 1656 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:146179367" variation 1661 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138799361" variation 1668 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:142813836" variation 1692 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200849554" variation 1698 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371096421" variation 1708 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147058580" variation 1724 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372897235" variation 1732 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372318760" variation 1748 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138234810" variation 1774 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:376332419" variation 1821 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:369647186" variation 1829 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:372009871" variation 1842 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:375200446" variation 1888 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:369331349" variation 1891 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:372494707" variation 1896 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:149459247" variation 1920 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:201968625" variation 1946 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:79308763" variation 1955 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201113386" variation 1978 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:140210209" variation 1979 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:144256388" variation 1981 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:148720535" variation 2020 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:145699923" variation 2035 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:75997823" variation 2150 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:45622835" variation 2197 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:147740049" variation 2306 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:41267923" variation 2336 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:140968699" variation 2351 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:190991772" variation 2395 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:181403362" variation 2444 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:142399461" variation 2492 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:80165853" variation 2538 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:9393721" variation 2568 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:151275014" variation 2595 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:76504501" variation 2739 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:185627402" variation 2763 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:140483657" variation 2774 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150406471" variation 2839 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:374762838" variation 2844 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:367610347" STS 2854..2980 /gene="BTN3A3" /gene_synonym="BTF3" /standard_name="WI-14381" /db_xref="UniSTS:69485" variation 2894..2895 /gene="BTN3A3" /gene_synonym="BTF3" /replace="" /replace="a" /db_xref="dbSNP:113625452" variation 2950 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:9770" variation 2951 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:141194871" variation 2958 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:189698449" variation 2959 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:144928044" variation 3001 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:41267925" ORIGIN
aatcaaaaaactaattcttccaaaaagagattgttattattcctcacaataaccagatagcctctgctttctttttcctttcttcggaatgagagactcaaccataatagaaagaatggagaactattaaccaccattcttcagtgggctgtgattttcagaggggaatactaagaaatggttttccatactggaacccaaaggtaaagacactcaaggacagacatttttggcagagcatagatgaaaatggcaagttccctggctttccttctgctcaactttcatgtctccctcttcttggtccagctgctcactccttgctcagctcagttttctgtgcttggaccctctgggcccatcctggccatggtgggtgaagacgctgatctgccctgtcacctgttcccgaccatgagtgcagagaccatggagctgaggtgggtgagttccagcctaaggcaggtggtgaacgtgtatgcagatggaaaggaagtggaagacaggcagagtgcaccgtatcgagggagaacttcgattctgcgggatggcatcactgcagggaaggctgctctccgaatacacaacgtcacagcctctgacagtggaaagtacttgtgttatttccaagatggtgacttctacgaaaaagccctggtggagctgaaggttgcagcattgggttctgatcttcacattgaagtgaagggttatgaggatggagggatccatctggagtgcaggtccactggctggtacccccaaccccaaataaagtggagcgacaccaagggagagaacatcccggctgtggaagcacctgtggttgcagatggagtgggcctgtatgcagtagcagcatctgtgatcatgagaggcagctctggtgggggtgtatcctgcatcatcagaaattccctcctcggcctggaaaagacagccagcatatccatcgcagaccccttcttcaggagcgcccagccctggatcgcggccctggcagggaccctgcctatctcgttgctgcttctcgcaggagccagttacttcttgtggagacaacagaaggaaaaaattgctctgtccagggagacagaaagagagcgagagatgaaagaaatgggatacgctgcaacagagcaagaaataagcctaagagagaagctccaggaggaactcaagtggaggaaaatccagtacatggctcgtggagagaagtctttggcctatcatgaatggaaaatggccctcttcaaacctgcggatgtgattctggatccagacacggcaaacgccatcctccttgtttctgaggaccagaggagtgtgcagcgtgctgaagagccgcgggatctgccagacaaccctgagagatttgaatggcgttactgtgtccttggctgtgaaaacttcacatcagggagacattactgggaggtggaagtgggggacagaaaagagtggcatattggggtatgtagtaagaacgtggagaggaaaaaaggttgggtcaaaatgacaccggagaacggatactggactatgggcctgactgatgggaataagtatcgggctctcactgagcccagaaccaacctgaaacttcctgagcctcctaggaaagtggggatcttcctggactatgagactggagagatctcgttctataatgccacagatggatctcatatctacacctttccgcacgcctctttctctgagcctctatatcctgttttcagaattttgaccttggagcccactgccctgaccatttgcccaataccaaaagaagtagagagttcccccgatcctgacctagtgcctgatcattccctggagacaccactgaccccgggcttagctaatgaaagtggggagcctcaggctgaagtaacatctctgcttctccctgcccaccctggagctgaggtctccccttctgcaacaaccaatcagaaccataagctacaggcacgcactgaagcactttactgatattcattccattattccatatgacagttgttttgagtttcgtaccaccttattgtccccttatacagataaggaaactggggtgcagaaaggtgaattaactttacaaagtagacatgacaagtgaacagcagagctgggatctaaacagcaataactaacattaacagagaatttaaaatgttcttagtgctgtgttataagctttggtggatgtcactcctttaatcctcacaacaccctgtcgggtagtcatattttgcaagtatggaagctgaggcagggcaacatgaagtaacttacataactcatacagtaatttgtgcagttgggagatgttcagccttagtccctggctaattgcctgttcttttccagcctgattttttttcccacaggaagagcccacatgtagccctgaggtttccttcccaggacagctgcagggtagagatcattttaagtgcttgtggagttgacatccctattgactctttcccagctgatatcagagacttagacccagcactccttggattagctctgcagagtgtcttggttgagagaataacctcatagtaccaacatgacatgtgacttggaaagagactagaggccacacttgataaatcatggggcacagatatgttcccacccaacaaatgtgataagtgattgtgcagccagagccagccttccttcaatcaaggtttccaggcagagcaaataccctagagattctctgtgatataggaaatttggatcaaggaagctaaaagaattacagggatgtttttaatcccactatggactcagtctcctggaaataggtctgtccactcctggtcattggtggatgttaaacccatattcctttcaactgctgcctgctagggaaaactgctcctcattatcatcactattattgctcaccactgtatcccctctacttggcaagtggttgtcaagttctagttgttcaataaatgtgttaataatgcttaaaaaaaaaaaaaaaaaa
//
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
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