2024-03-29 07:55:08, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001242803 2364 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens butyrophilin, subfamily 3, member A3 (BTN3A3), transcript variant 3, mRNA. ACCESSION NM_001242803 VERSION NM_001242803.1 GI:338797728 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 2364) 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 2364) 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 2364) 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 2364) 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 2364) 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 DA445999.1, BX341863.2 and BC015815.2. 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 (3) lacks several exons in two regions, but the open reading frame is retained, compared to variant 1. The encoded isoform (c) has a shorter N-terminus and lacks an internal segment, compared to isoform a. ##Evidence-Data-START## Transcript exon combination :: BX341863.2 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025088 [ECO:0000348] ##Evidence-Data-END## PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-88 DA445999.1 1-88 89-849 BX341863.2 5-765 850-2364 BC015815.2 1442-2956 FEATURES Location/Qualifiers source 1..2364 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="6" /map="6p21.3" gene 1..2364 /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" misc_feature 108..110 /gene="BTN3A3" /gene_synonym="BTF3" /note="upstream in-frame stop codon" variation 121 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:117832370" exon 178..525 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 202 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:375578358" CDS 219..1343 /gene="BTN3A3" /gene_synonym="BTF3" /note="isoform c is encoded by transcript variant 3; butyrophilin 3" /codon_start=1 /product="butyrophilin subfamily 3 member A3 isoform c" /protein_id="NP_001229732.1" /db_xref="GI:338797729" /db_xref="GeneID:10384" /db_xref="HGNC:1140" /db_xref="MIM:613595" /translation="
MVGEDADLPCHLFPTMSAETMELRWVSSSLRQVVNVYADGKEVEDRQSAPYRGRTSILRDGITAGKAALRIHNVTASDSGKYLCYFQDGDFYEKALVELKVAEWRKIQYMARGEKSLAYHEWKMALFKPADVILDPDTANAILLVSEDQRSVQRAEEPRDLPDNPERFEWRYCVLGCENFTSGRHYWEVEVGDRKEWHIGVCSKNVERKKGWVKMTPENGYWTMGLTDGNKYRALTEPRTNLKLPEPPRKVGIFLDYETGEISFYNATDGSHIYTFPHASFSEPLYPVFRILTLEPTALTICPIPKEVESSPDPDLVPDHSLETPLTPGLANESGEPQAEVTSLLLPAHPGAEVSPSATTNQNHKLQARTEALY
" misc_feature 225..524 /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 231..470 /gene="BTN3A3" /gene_synonym="BTF3" /note="Immunoglobulin V-Type; Region: IGv; smart00406" /db_xref="CDD:197704" misc_feature order(273..278,333..335,366..368,477..479,483..500) /gene="BTN3A3" /gene_synonym="BTF3" /note="antigen binding site; other site" /db_xref="CDD:143190" misc_feature 603..758 /gene="BTN3A3" /gene_synonym="BTF3" /note="associated with SPRY domains; Region: PRY; smart00589" /db_xref="CDD:128857" misc_feature 762..1130 /gene="BTN3A3" /gene_synonym="BTF3" /note="Domain in SPla and the RYanodine Receptor; Region: SPRY; smart00449" /db_xref="CDD:128725" variation 234 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:376102561" variation 259 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:368285328" variation 260 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:77474489" variation 265 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200536472" variation 278 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371864834" variation 296 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201309184" variation 324 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:137957846" variation 351 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:375239049" variation 368 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147078433" variation 372 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:376234984" variation 385 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138755245" variation 393 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:149312684" variation 426 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372313829" exon 526..552 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 546 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:202118130" variation 547 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:140111422" variation 548 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150366659" exon 553..579 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 558 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:138105205" variation 564 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:74640395" variation 565 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:79652472" exon 580..606 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 581 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:201134941" exon 607..2347 /gene="BTN3A3" /gene_synonym="BTF3" /inference="alignment:Splign:1.39.8" variation 608 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200780915" variation 631 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:199818322" variation 633 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:112698147" variation 635 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:368263332" variation 638 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:201403401" variation 643 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:370679491" variation 652 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:374373356" variation 666 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:149504053" variation 673 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:114347679" variation 674 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:200995489" variation 692 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:141739374" variation 710 /gene="BTN3A3" /gene_synonym="BTF3" /replace="" /replace="c" /db_xref="dbSNP:35279486" variation 728 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:116318960" variation 729 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200026955" variation 730 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147489251" variation 740 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:139835450" variation 744 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:367977572" variation 770 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371833271" variation 773 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:142830190" variation 776 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:150687753" variation 802 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150755364" variation 807 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:375702813" variation 850 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:149823309" variation 851 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:367714257" variation 867 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:113551647" variation 868 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:146835625" variation 869 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:140664333" variation 874 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:139072503" variation 884 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:372614651" variation 896 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:143237800" variation 913 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:146699487" variation 915 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:148819206" variation 923 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:143460142" variation 940 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:151008942" variation 953 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:370056298" variation 956 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:374128957" variation 972 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:368736832" variation 975 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:189581403" variation 978 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:181680390" variation 989 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:140904550" variation 999 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:369319317" variation 1001 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:146179367" variation 1006 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138799361" variation 1013 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:142813836" variation 1037 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:200849554" variation 1043 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:371096421" variation 1053 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:147058580" variation 1069 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372897235" variation 1077 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:372318760" variation 1093 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:138234810" variation 1119 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:376332419" variation 1166 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:369647186" variation 1174 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:372009871" variation 1187 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:375200446" variation 1233 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:369331349" variation 1236 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:372494707" variation 1241 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:149459247" variation 1265 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:201968625" variation 1291 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:79308763" variation 1300 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:201113386" variation 1323 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:140210209" variation 1324 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:144256388" variation 1326 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:148720535" variation 1365 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="t" /db_xref="dbSNP:145699923" variation 1380 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:75997823" variation 1495 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:45622835" variation 1542 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:147740049" variation 1651 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:41267923" variation 1681 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:140968699" variation 1696 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:190991772" variation 1740 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:181403362" variation 1789 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:142399461" variation 1837 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:80165853" variation 1883 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:9393721" variation 1913 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:151275014" variation 1940 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:76504501" variation 2084 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="c" /db_xref="dbSNP:185627402" variation 2108 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:140483657" variation 2119 /gene="BTN3A3" /gene_synonym="BTF3" /replace="a" /replace="g" /db_xref="dbSNP:150406471" variation 2184 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="t" /db_xref="dbSNP:374762838" variation 2189 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:367610347" STS 2199..2325 /gene="BTN3A3" /gene_synonym="BTF3" /standard_name="WI-14381" /db_xref="UniSTS:69485" variation 2239..2240 /gene="BTN3A3" /gene_synonym="BTF3" /replace="" /replace="a" /db_xref="dbSNP:113625452" variation 2295 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:9770" variation 2296 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:141194871" variation 2303 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:189698449" variation 2304 /gene="BTN3A3" /gene_synonym="BTF3" /replace="c" /replace="g" /db_xref="dbSNP:144928044" variation 2346 /gene="BTN3A3" /gene_synonym="BTF3" /replace="g" /replace="t" /db_xref="dbSNP:41267925" ORIGIN
aatcaaaaaactaattcttccaaaaagagattgttattattcctcacaataaccagatagcctctgctttctttttcctttcttcggaatgagagactcaaccataatagaaagaatggagaactattaaccaccattcttcagtgggctgtgattttcagaggggaatactaagaactcagttttctgtgcttggaccctctgggcccatcctggccatggtgggtgaagacgctgatctgccctgtcacctgttcccgaccatgagtgcagagaccatggagctgaggtgggtgagttccagcctaaggcaggtggtgaacgtgtatgcagatggaaaggaagtggaagacaggcagagtgcaccgtatcgagggagaacttcgattctgcgggatggcatcactgcagggaaggctgctctccgaatacacaacgtcacagcctctgacagtggaaagtacttgtgttatttccaagatggtgacttctacgaaaaagccctggtggagctgaaggttgcagagtggaggaaaatccagtacatggctcgtggagagaagtctttggcctatcatgaatggaaaatggccctcttcaaacctgcggatgtgattctggatccagacacggcaaacgccatcctccttgtttctgaggaccagaggagtgtgcagcgtgctgaagagccgcgggatctgccagacaaccctgagagatttgaatggcgttactgtgtccttggctgtgaaaacttcacatcagggagacattactgggaggtggaagtgggggacagaaaagagtggcatattggggtatgtagtaagaacgtggagaggaaaaaaggttgggtcaaaatgacaccggagaacggatactggactatgggcctgactgatgggaataagtatcgggctctcactgagcccagaaccaacctgaaacttcctgagcctcctaggaaagtggggatcttcctggactatgagactggagagatctcgttctataatgccacagatggatctcatatctacacctttccgcacgcctctttctctgagcctctatatcctgttttcagaattttgaccttggagcccactgccctgaccatttgcccaataccaaaagaagtagagagttcccccgatcctgacctagtgcctgatcattccctggagacaccactgaccccgggcttagctaatgaaagtggggagcctcaggctgaagtaacatctctgcttctccctgcccaccctggagctgaggtctccccttctgcaacaaccaatcagaaccataagctacaggcacgcactgaagcactttactgatattcattccattattccatatgacagttgttttgagtttcgtaccaccttattgtccccttatacagataaggaaactggggtgcagaaaggtgaattaactttacaaagtagacatgacaagtgaacagcagagctgggatctaaacagcaataactaacattaacagagaatttaaaatgttcttagtgctgtgttataagctttggtggatgtcactcctttaatcctcacaacaccctgtcgggtagtcatattttgcaagtatggaagctgaggcagggcaacatgaagtaacttacataactcatacagtaatttgtgcagttgggagatgttcagccttagtccctggctaattgcctgttcttttccagcctgattttttttcccacaggaagagcccacatgtagccctgaggtttccttcccaggacagctgcagggtagagatcattttaagtgcttgtggagttgacatccctattgactctttcccagctgatatcagagacttagacccagcactccttggattagctctgcagagtgtcttggttgagagaataacctcatagtaccaacatgacatgtgacttggaaagagactagaggccacacttgataaatcatggggcacagatatgttcccacccaacaaatgtgataagtgattgtgcagccagagccagccttccttcaatcaaggtttccaggcagagcaaataccctagagattctctgtgatataggaaatttggatcaaggaagctaaaagaattacagggatgtttttaatcccactatggactcagtctcctggaaataggtctgtccactcctggtcattggtggatgttaaacccatattcctttcaactgctgcctgctagggaaaactgctcctcattatcatcactattattgctcaccactgtatcccctctacttggcaagtggttgtcaagttctagttgttcaataaatgtgttaataatgcttaaaaaaaaaaaaaaaaaa
//
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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