2024-03-29 08:19:45, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_033229 2241 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens tripartite motif containing 15 (TRIM15), mRNA. ACCESSION NM_033229 VERSION NM_033229.2 GI:149193330 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 2241) AUTHORS McElroy,J.P., Cree,B.A., Caillier,S.J., Gregersen,P.K., Herbert,J., Khan,O.A., Freudenberg,J., Lee,A., Bridges,S.L. Jr., Hauser,S.L., Oksenberg,J.R. and Gourraud,P.A. TITLE Refining the association of MHC with multiple sclerosis in African Americans JOURNAL Hum. Mol. Genet. 19 (15), 3080-3088 (2010) PUBMED 20466734 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 2 (bases 1 to 2241) AUTHORS Barcellos,L.F., May,S.L., Ramsay,P.P., Quach,H.L., Lane,J.A., Nititham,J., Noble,J.A., Taylor,K.E., Quach,D.L., Chung,S.A., Kelly,J.A., Moser,K.L., Behrens,T.W., Seldin,M.F., Thomson,G., Harley,J.B., Gaffney,P.M. and Criswell,L.A. TITLE High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions JOURNAL PLoS Genet. 5 (10), E1000696 (2009) PUBMED 19851445 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 3 (bases 1 to 2241) AUTHORS Uchil,P.D., Quinlan,B.D., Chan,W.T., Luna,J.M. and Mothes,W. TITLE TRIM E3 ligases interfere with early and late stages of the retroviral life cycle JOURNAL PLoS Pathog. 4 (2), E16 (2008) PUBMED 18248090 REMARK GeneRIF: Downregulation of TRIM11 and TRIM15 enhanced virus release suggesting that these proteins contribute to the endogenous restriction of retroviruses in cells. REFERENCE 4 (bases 1 to 2241) AUTHORS Lamesch,P., Li,N., Milstein,S., Fan,C., Hao,T., Szabo,G., Hu,Z., Venkatesan,K., Bethel,G., Martin,P., Rogers,J., Lawlor,S., McLaren,S., Dricot,A., Borick,H., Cusick,M.E., Vandenhaute,J., Dunham,I., Hill,D.E. and Vidal,M. TITLE hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes JOURNAL Genomics 89 (3), 307-315 (2007) PUBMED 17207965 REFERENCE 5 (bases 1 to 2241) AUTHORS Shiina,T., Ota,M., Shimizu,S., Katsuyama,Y., Hashimoto,N., Takasu,M., Anzai,T., Kulski,J.K., Kikkawa,E., Naruse,T., Kimura,N., Yanagiya,K., Watanabe,A., Hosomichi,K., Kohara,S., Iwamoto,C., Umehara,Y., Meyer,A., Wanner,V., Sano,K., Macquin,C., Ikeo,K., Tokunaga,K., Gojobori,T., Inoko,H. and Bahram,S. TITLE Rapid evolution of major histocompatibility complex class I genes in primates generates new disease alleles in humans via hitchhiking diversity JOURNAL Genetics 173 (3), 1555-1570 (2006) PUBMED 16702430 REFERENCE 6 (bases 1 to 2241) AUTHORS Reymond,A., Meroni,G., Fantozzi,A., Merla,G., Cairo,S., Luzi,L., Riganelli,D., Zanaria,E., Messali,S., Cainarca,S., Guffanti,A., Minucci,S., Pelicci,P.G. and Ballabio,A. TITLE The tripartite motif family identifies cell compartments JOURNAL EMBO J. 20 (9), 2140-2151 (2001) PUBMED 11331580 REFERENCE 7 (bases 1 to 2241) AUTHORS Harada,H., Harada,Y., O'Brien,D.P., Rice,D.S., Naeve,C.W. and Downing,J.R. TITLE HERF1, a novel hematopoiesis-specific RING finger protein, is required for terminal differentiation of erythroid cells JOURNAL Mol. Cell. Biol. 19 (5), 3808-3815 (1999) PUBMED 10207104 REFERENCE 8 (bases 1 to 2241) AUTHORS Gruen,J.R., Nalabolu,S.R., Chu,T.W., Bowlus,C., Fan,W.F., Goei,V.L., Wei,H., Sivakamasundari,R., Liu,Y., Xu,H.X., Parimoo,S., Nallur,G., Ajioka,R., Shukla,H., Bray-Ward,P., Pan,J. and Weissman,S.M. TITLE A transcription map of the major histocompatibility complex (MHC) class I region JOURNAL Genomics 36 (1), 70-85 (1996) PUBMED 8812418 REFERENCE 9 (bases 1 to 2241) AUTHORS Goei,V.L., Parimoo,S., Capossela,A., Chu,T.W. and Gruen,J.R. TITLE Isolation of novel non-HLA gene fragments from the hemochromatosis region (6p21.3) by cDNA hybridization selection JOURNAL Am. J. Hum. Genet. 54 (2), 244-251 (1994) PUBMED 8304341 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BP270476.1, AL669914.2, BC038585.1, U34249.1 and AI739162.1. On Jun 20, 2007 this sequence version replaced gi:15100169. Summary: The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to the cytoplasm. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]. ##Evidence-Data-START## Transcript exon combination :: U34249.1, AK290280.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support ERS025084, ERS025088 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-366 BP270476.1 1-366 367-367 AL669914.2 158205-158205 368-399 BP270476.1 368-399 400-1449 BC038585.1 1-1050 1450-2092 U34249.1 1464-2106 2093-2220 AI739162.1 1-128 c 2221-2241 U34249.1 2235-2255 FEATURES Location/Qualifiers source 1..2241 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="6" /map="6p21.3" gene 1..2241 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="tripartite motif containing 15" /db_xref="GeneID:89870" /db_xref="HGNC:16284" exon 1..860 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /inference="alignment:Splign:1.39.8" variation 141 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="g" /replace="t" /db_xref="dbSNP:17188113" variation 181 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="" /replace="a" /db_xref="dbSNP:367652914" variation 237 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="c" /db_xref="dbSNP:371744467" variation 238 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="g" /replace="t" /db_xref="dbSNP:189105911" variation 295 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:372667978" variation 314 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="c" /db_xref="dbSNP:146207681" variation 336..337 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="" /replace="ctct" /db_xref="dbSNP:200720900" variation 348..349 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="" /replace="ctct" /db_xref="dbSNP:368841242" variation 349 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:62407492" variation 349 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="ctctttctctctctctgtctctc" /replace="t" /db_xref="dbSNP:369656818" variation 367 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:9261536" variation 367 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="ctctctctctctgtctctc" /replace="t" /db_xref="dbSNP:369834849" misc_feature 441..443 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="upstream in-frame stop codon" variation 447 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:376378714" CDS 480..1877 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="zinc finger protein 178; tripartite motif-containing 15; RING finger protein 93; zinc finger protein B7" /codon_start=1 /product="tripartite motif-containing protein 15" /protein_id="NP_150232.2" /db_xref="GI:149193331" /db_xref="CCDS:CCDS4677.1" /db_xref="GeneID:89870" /db_xref="HGNC:16284" /translation="
MPATPSLKVVHELPACTLCAGPLEDAVTIPCGHTFCRLCLPALSQMGAQSSGKILLCPLCQEEEQAETPMAPVPLGPLGETYCEEHGEKIYFFCENDAEFLCVFCREGPTHQAHTVGFLDEAIQPYRDRLRSRLEALSTERDEIEDVKCQEDQKLQVLLTQIESKKHQVETAFERLQQELEQQRCLLLARLRELEQQIWKERDEYITKVSEEVTRLGAQVKELEEKCQQPASELLQDVRVNQSRCEMKTFVSPEAISPDLVKKIRDFHRKILTLPEMMRMFSENLAHHLEIDSGVITLDPQTASRSLVLSEDRKSVRYTRQKKSLPDSPLRFDGLPAVLGFPGFSSGRHRWQVDLQLGDGGGCTVGVAGEGVRRKGEMGLSAEDGVWAVIISHQQCWASTSPGTDLPLSEIPRGVRVALDYEAGQVTLHNAQTQEPIFTFTASFSGKVFPFFAVWKKGSCLTLKG
" misc_feature 525..668 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="RING-finger (Really Interesting New Gene) domain, a specialized type of Zn-finger of 40 to 60 residues that binds two atoms of zinc; defined by the 'cross-brace' motif C-X2-C-X(9-39)-C-X(1-3)- H-X(2-3)-(N/C/H)-X2-C-X(4-48)C-X2-C; probably involved in...; Region: RING; cd00162" /db_xref="CDD:29102" misc_feature order(525..527,534..536,570..572,576..578,585..587, 594..596,648..650,657..659) /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="cross-brace motif; other site" /db_xref="CDD:29102" misc_feature 720..836 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="B-Box-type zinc finger; zinc binding domain (CHC3H2); often present in combination with other motifs, like RING zinc finger, NHL motif, coiled-coil or RFP domain in functionally unrelated proteins, most likely mediating protein-protein interaction; Region: BBOX; cd00021" /db_xref="CDD:28905" misc_feature order(726..728,735..737,792..794,810..812) /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="Zn2+ binding site [ion binding]; other site" /db_xref="CDD:28905" misc_feature 1365..1511 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="SPRY-associated domain; Region: PRY; pfam13765" /db_xref="CDD:205938" misc_feature 1515..1859 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /note="Domain in SPla and the RYanodine Receptor; Region: SPRY; smart00449" /db_xref="CDD:128725" variation 486 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:201508191" variation 501 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:143628773" variation 521 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:35278640" variation 533 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="g" /replace="t" /db_xref="dbSNP:2523733" variation 541 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="g" /replace="t" /db_xref="dbSNP:373721924" variation 542 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:144796171" variation 545 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="g" /replace="t" /db_xref="dbSNP:11961941" variation 561 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:368737286" variation 564 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:17194460" variation 603 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:17194467" variation 611 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:372226825" variation 632 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:138173429" variation 699 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:200404814" variation 729 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:17194474" variation 761 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:143039782" variation 803..804 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="c" /db_xref="dbSNP:2857452" variation 804 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:2523732" variation 805 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:144365165" exon 861..956 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /inference="alignment:Splign:1.39.8" variation 864 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="c" /db_xref="dbSNP:373372000" variation 865 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:376718713" variation 868 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="g" /replace="t" /db_xref="dbSNP:201369873" variation 873 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:139358870" variation 877 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="g" /replace="t" /db_xref="dbSNP:143173321" variation 895 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:56866777" variation 917 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="t" /db_xref="dbSNP:140385648" exon 957..1187 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /inference="alignment:Splign:1.39.8" variation 963 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:61746149" variation 1012 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:113222785" variation 1020 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:113787537" variation 1028 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:150718462" variation 1030 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:61738774" variation 1098 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="t" /db_xref="dbSNP:369181343" variation 1110 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:149881430" variation 1123 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:182100536" variation 1182 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:34823152" exon 1188..1210 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /inference="alignment:Splign:1.39.8" variation 1206 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:370109967" variation 1208 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:141139052" exon 1211..1326 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /inference="alignment:Splign:1.39.8" variation 1223 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:377477000" variation 1225 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:371160070" variation 1226 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:61744342" variation 1255 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:113942323" variation 1259 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:374562707" variation 1288 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:115839038" exon 1327..1359 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /inference="alignment:Splign:1.39.8" exon 1360..2224 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /inference="alignment:Splign:1.39.8" variation 1381 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:201819032" variation 1450 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:929156" variation 1451 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:143734427" variation 1471 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="g" /replace="t" /db_xref="dbSNP:199747350" variation 1491 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:375119144" variation 1545 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:200479072" variation 1589 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:191507786" variation 1608 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:71561356" variation 1667 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="c" /db_xref="dbSNP:375289482" variation 1722 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:115649931" variation 1766 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:142991113" variation 1792 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="t" /db_xref="dbSNP:1063276" variation 1808 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:1063277" variation 1812 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="t" /db_xref="dbSNP:1063278" variation 1820 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:1063279" variation 1918 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:150264994" variation 1923 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:369877929" variation 1933 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:370143829" variation 2031..2034 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="" /replace="ttat" /db_xref="dbSNP:371041335" variation 2093 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="t" /db_xref="dbSNP:1063280" variation 2116 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="a" /replace="g" /db_xref="dbSNP:138979251" variation 2161 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="c" /replace="g" /db_xref="dbSNP:149454547" polyA_signal 2196..2201 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" variation 2205 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" /replace="" /replace="t" /db_xref="dbSNP:375616592" polyA_site 2224 /gene="TRIM15" /gene_synonym="RNF93; ZNF178; ZNFB7" ORIGIN
actttgatgctgtgggcacgcctcagagccagaagtttatggctcccacctgctcaatctgacaggaagcttctgctccccagttctccccagccactgtggtctacagattccaggaaacccatccccctgtgacctcatggtgtgctctgttctccaccctagggaccagaaggagccaggagtaaagaactggcttacttggccgccactgggaaattctgggtaattcgagacgccctggaatttggacccactccgctgataggtggtggccagggttctagggaacacaagaggcggagccaggtggcttccctgtgctggcattcttgcctctctctctctttctctctctctgtctcttagccttgcagccgtttccctctgcgattcatgtaagtgtgactcgatttcagggaaagggaactcgcgtgggctgaggagaccggagtggacgggctggggaaggcaccgtgatgcccgcaaccccgtccctgaaggtggtccatgagctgcctgcctgtaccctctgtgcggggccgctggaggatgcggtgaccattccctgtggacacaccttctgccggctctgcctccccgcgctctcccagatgggggcccaatcctcgggcaagatcctgctctgcccgctctgccaagaggaggagcaggcagagactcccatggcccctgtgcccctgggcccgctgggagaaacttactgcgaggagcacggcgagaagatctacttcttctgcgagaacgatgccgagttcctctgtgtgttctgcagggagggtcccacgcaccaggcgcacaccgtggggttcctggacgaggccattcagccctaccgggatcgtctcaggagtcgactggaagctctgagcacggagagagatgagattgaggatgtaaagtgtcaagaagaccagaagcttcaagtgctgctgactcagatcgaaagcaagaagcatcaggtggaaacagcttttgagaggctgcagcaggagctggagcagcagcgatgtctcctgctggccaggctgagggagctggagcagcagatttggaaggagagggatgaatatatcacaaaggtctctgaggaagtcacccggcttggagcccaggtcaaggagctggaggagaagtgtcagcagccagcaagtgagcttctacaagatgtcagagtcaaccagagcaggtgtgagatgaagacttttgtgagtcctgaggccatttctcctgaccttgtcaagaagatccgtgatttccacaggaaaatactcaccctcccagagatgatgaggatgttctcagaaaacttggcgcatcatctggaaatagattcaggggtcatcactctggaccctcagaccgccagccggagcctggttctctcggaagacaggaagtcagtgaggtacacccggcagaagaagagcctgccagacagccccctgcgcttcgacggcctcccggcggttctgggcttcccgggcttctcctccgggcgccaccgctggcaggttgacctgcagctgggcgacggcggcggctgcacggtgggggtggccggggagggggtgaggaggaagggagagatgggactcagcgccgaggacggcgtctgggccgtgatcatctcgcaccagcagtgctgggccagcacctccccgggcaccgacctgccgctgagcgagatcccgcgcggcgtgagagtcgccctggactacgaggcggggcaggtgaccctccacaacgcccagacccaggagcccatcttcaccttcactgcctctttctccggcaaagtcttccctttctttgccgtctggaaaaaaggttcctgccttacgctgaaaggctgaagtggggcgcgcgaagggcggcgaagcggagacggcggctctccgggatccagctccgcccctggccagtgtgcggcccgggggctccctgtgcccgcgtgaggcgagagaacaggggacttgagtctcgaacagcggttgtttttactttatttatcttaggccctcagctccctgacgtcctgagcctccctgtgacgctctggccttctctgtacctcagagtgcagaaccacagacggcttcggctgtgcctagggcaacagccaacctaggagccagcgggctttcggggaaaaaaaagaaaaagacatctaaaataaaatgtttaaactgtttcaaaataaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:89870 -> Molecular function: GO:0008270 [zinc ion binding] evidence: IEA GeneID:89870 -> Biological process: GO:0007500 [mesodermal cell fate determination] evidence: TAS GeneID:89870 -> Cellular component: GO:0005622 [intracellular] evidence: IEA
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