2024-11-23 18:31:38, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_018445 1250 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens VCP-interacting membrane protein (VIMP), transcript variant 2, mRNA. ACCESSION NM_018445 VERSION NM_018445.4 GI:45439347 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 1250) AUTHORS Christensen,L.C., Jensen,N.W., Vala,A., Kamarauskaite,J., Johansson,L., Winther,J.R., Hofmann,K., Teilum,K. and Ellgaard,L. TITLE The human selenoprotein VCP-interacting membrane protein (VIMP) is non-globular and harbors a reductase function in an intrinsically disordered region JOURNAL J. Biol. Chem. 287 (31), 26388-26399 (2012) PUBMED 22700979 REMARK GeneRIF: the redox properties observed for recombinant VIMP are compatible with a function as a reductase REFERENCE 2 (bases 1 to 1250) AUTHORS Fradejas,N., Serrano-Perez Mdel,C., Tranque,P. and Calvo,S. TITLE Selenoprotein S expression in reactive astrocytes following brain injury JOURNAL Glia 59 (6), 959-972 (2011) PUBMED 21456042 REMARK GeneRIF: Upregulation of SelS expression in reactive astrocytes reveals a new protective role for SelS against inflammation and endoplasmic reticulum stress that can be relevant to astrocyte function. REFERENCE 3 (bases 1 to 1250) AUTHORS Olsson,M., Olsson,B., Jacobson,P., Thelle,D.S., Bjorkegren,J., Walley,A., Froguel,P., Carlsson,L.M. and Sjoholm,K. TITLE Expression of the selenoprotein S (SELS) gene in subcutaneous adipose tissue and SELS genotype are associated with metabolic risk factors JOURNAL Metab. Clin. Exp. 60 (1), 114-120 (2011) PUBMED 20619427 REMARK GeneRIF: a role for SELS in the development of metabolic disease, especially in the context of insulin resistance. GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 4 (bases 1 to 1250) AUTHORS Sutherland,A., Kim,D.H., Relton,C., Ahn,Y.O. and Hesketh,J. TITLE Polymorphisms in the selenoprotein S and 15-kDa selenoprotein genes are associated with altered susceptibility to colorectal cancer JOURNAL Genes Nutr 5 (3), 215-223 (2010) PUBMED 21052528 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 5 (bases 1 to 1250) AUTHORS Meplan,C., Hughes,D.J., Pardini,B., Naccarati,A., Soucek,P., Vodickova,L., Hlavata,I., Vrana,D., Vodicka,P. and Hesketh,J.E. TITLE Genetic variants in selenoprotein genes increase risk of colorectal cancer JOURNAL Carcinogenesis 31 (6), 1074-1079 (2010) PUBMED 20378690 REMARK GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 6 (bases 1 to 1250) AUTHORS Gao,Y., Feng,H.C., Walder,K., Bolton,K., Sunderland,T., Bishara,N., Quick,M., Kantham,L. and Collier,G.R. TITLE Regulation of the selenoprotein SelS by glucose deprivation and endoplasmic reticulum stress - SelS is a novel glucose-regulated protein JOURNAL FEBS Lett. 563 (1-3), 185-190 (2004) PUBMED 15063746 REMARK GeneRIF: SELS is regulated by glucose deprivation and endoplasmic reticulum stress. It is a glucose-regulated protein. REFERENCE 7 (bases 1 to 1250) AUTHORS Kryukov,G.V., Castellano,S., Novoselov,S.V., Lobanov,A.V., Zehtab,O., Guigo,R. and Gladyshev,V.N. TITLE Characterization of mammalian selenoproteomes JOURNAL Science 300 (5624), 1439-1443 (2003) PUBMED 12775843 REFERENCE 8 (bases 1 to 1250) AUTHORS Gao,Y., Walder,K., Sunderland,T., Kantham,L., Feng,H.C., Quick,M., Bishara,N., de Silva,A., Augert,G., Tenne-Brown,J. and Collier,G.R. TITLE Elevation in Tanis expression alters glucose metabolism and insulin sensitivity in H4IIE cells JOURNAL Diabetes 52 (4), 929-934 (2003) PUBMED 12663463 REFERENCE 9 (bases 1 to 1250) AUTHORS Walder,K., Kantham,L., McMillan,J.S., Trevaskis,J., Kerr,L., De Silva,A., Sunderland,T., Godde,N., Gao,Y., Bishara,N., Windmill,K., Tenne-Brown,J., Augert,G., Zimmet,P.Z. and Collier,G.R. TITLE Tanis: a link between type 2 diabetes and inflammation? JOURNAL Diabetes 51 (6), 1859-1866 (2002) PUBMED 12031974 REFERENCE 10 (bases 1 to 1250) AUTHORS Hu,R.M., Han,Z.G., Song,H.D., Peng,Y.D., Huang,Q.H., Ren,S.X., Gu,Y.J., Huang,C.H., Li,Y.B., Jiang,C.L., Fu,G., Zhang,Q.H., Gu,B.W., Dai,M., Mao,Y.F., Gao,G.F., Rong,R., Ye,M., Zhou,J., Xu,S.H., Gu,J., Shi,J.X., Jin,W.R., Zhang,C.K., Wu,T.M., Huang,G.Y., Chen,Z., Chen,M.D. and Chen,J.L. TITLE Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning JOURNAL Proc. Natl. Acad. Sci. U.S.A. 97 (17), 9543-9548 (2000) PUBMED 10931946 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BG829960.1, BC005840.2, BQ014190.1 and BI494034.1. On Mar 15, 2004 this sequence version replaced gi:42734439. Summary: This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Studies suggest that this protein may regulate cytokine production, and thus play a key role in the control of the inflammatory response. Two alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]. Transcript Variant: This variant (2) has a different 3' UTR compared to variant 1. Transcript variants 1 and 2 encode the same protein. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BG723489.1, AK026455.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025084, ERS025088 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## protein contains selenocysteine :: PMID: 12775843 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-52 BG829960.1 26-77 53-1224 BC005840.2 1-1172 1225-1231 BQ014190.1 17-23 c 1232-1250 BI494034.1 1-19 c FEATURES Location/Qualifiers source 1..1250 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="15" /map="15q26.3" gene 1..1250 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /note="VCP-interacting membrane protein" /db_xref="GeneID:55829" /db_xref="HGNC:30396" /db_xref="MIM:607918" exon 1..154 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /inference="alignment:Splign:1.39.8" misc_feature 10..12 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /note="upstream in-frame stop codon" CDS 79..648 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /codon_start=1 /transl_except=(pos:640..642,aa:Sec) /product="selenoprotein S" /protein_id="NP_060915.2" /db_xref="GI:33285002" /db_xref="CCDS:CCDS53979.1" /db_xref="GeneID:55829" /db_xref="HGNC:30396" /db_xref="MIM:607918" /translation="
MERQEESLSARPALETEGLRFLHTTVGSLLATYGWYIVFSCILLYVVFQKLSARLRALRQRQLDRAAAAVEPDVVVKRQEALAAARLKMQEELNAQVEKHKEKLKQLEEEKRRQKIEMWDSMQEGKSYKGNAKKPQEEDSPGPSTSSVLKRKSDRKPLRGGGYNPLSGEGGGACSWRPGRRGPSSGGUG
" misc_feature 85..606 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /note="Selenoprotein S (SelS); Region: Selenoprotein_S; pfam06936" /db_xref="CDD:148511" misc_feature 160..222 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /inference="non-experimental evidence, no additional details recorded" /note="propagated from UniProtKB/Swiss-Prot (Q9BQE4.3); transmembrane region" misc_feature 496..498 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /experiment="experimental evidence, no additional details recorded" /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot (Q9BQE4.3); phosphorylation site" misc_feature 640..642 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /note="Selenocysteine; other site" exon 155..289 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /inference="alignment:Splign:1.39.8" exon 290..396 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /inference="alignment:Splign:1.39.8" exon 397..486 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /inference="alignment:Splign:1.39.8" exon 487..562 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /inference="alignment:Splign:1.39.8" variation 496 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /replace="a" /replace="g" /db_xref="dbSNP:200236506" exon 563..1234 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /inference="alignment:Splign:1.39.8" STS 960..1082 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /standard_name="RH46969" /db_xref="UniSTS:6952" polyA_site 1144 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /experiment="experimental evidence, no additional details recorded" polyA_signal 1203..1208 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" polyA_site 1224 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /experiment="experimental evidence, no additional details recorded" polyA_site 1231 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" /experiment="experimental evidence, no additional details recorded" polyA_site 1234 /gene="VIMP" /gene_synonym="AD-015; ADO15; SBBI8; SELS; SEPS1" ORIGIN
acgtgtgcgtaggagcgcaccggaagcgcccggctggaggcgcggcggcagggctgggcggcggcggcggcggcggtcatggaacgccaagaggagtctctgtccgcgcggccggccctggagaccgaggggctgcgcttcctgcacaccacggtgggctccctgctggccacctatggctggtacatcgtcttcagctgcatccttctctacgtggtctttcagaagctttccgcccggctaagagccttgaggcagaggcagctggaccgagctgcggctgctgtggaacctgatgttgttgttaaacgacaagaagctttagcagctgctcgactgaaaatgcaagaagaactaaatgcgcaagttgaaaagcataaggaaaaactgaaacaacttgaagaagaaaaaaggagacagaagattgaaatgtgggacagcatgcaagaaggaaaaagttacaaaggaaatgcaaagaagccccaggaggaagacagtcctgggccttccacttcatctgtcctgaaacggaaatcggacagaaagcctttgcggggaggaggttataacccgttgtctggtgaaggaggcggagcttgctcctggagacctggacgcagaggcccgtcatctggcggatgaggctaagaatcttgttagtgtcacttttgacattagcaagatgaacccttaaccctcgattcaattgccttacgcacgcttttcacagtgactagccaaggggaggtggggttgatttctgttcctaactacacctgcatatgtcagggctccagtcagcaaaaggtatagatgttgcctctaggcatgaggtcattggtcacattctacttggagacagtgattgcattcattgatttcatggttaattgctagttggtaggtaaaggcctctagatgattagcaatcttgataaaagaggcctagtaatgttcttttgaggttagaaatccttgctgctaggacagtctctgtgacaggttgcgttgaatgatgtcttccttatcaatggtgagcccaccagtgaggattactgatgtggacagttgatggggtttgtttctgtatatttatttttatgtacagaactttgtaaaaacgaaactatttaaaaaacaagaataacatttttagcatctttattcaaggagatttatggacttcaatttgtctatcaaacattaaatagctttttattacaacctctaactaaaaaaaaaaaaaaaaa
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ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:55829 -> Molecular function: GO:0004872 [receptor activity] evidence: NAS GeneID:55829 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:55829 -> Molecular function: GO:0008430 [selenium binding] evidence: IEA GeneID:55829 -> Molecular function: GO:0016209 [antioxidant activity] evidence: IDA GeneID:55829 -> Molecular function: GO:0019899 [enzyme binding] evidence: IPI GeneID:55829 -> Biological process: GO:0002865 [negative regulation of acute inflammatory response to antigenic stimulus] evidence: IMP GeneID:55829 -> Biological process: GO:0006111 [regulation of gluconeogenesis] evidence: TAS GeneID:55829 -> Biological process: GO:0006983 [ER overload response] evidence: IDA GeneID:55829 -> Biological process: GO:0006983 [ER overload response] evidence: IMP GeneID:55829 -> Biological process: GO:0009749 [response to glucose stimulus] evidence: IEP GeneID:55829 -> Biological process: GO:0030433 [ER-associated protein catabolic process] evidence: IDA GeneID:55829 -> Biological process: GO:0030968 [endoplasmic reticulum unfolded protein response] evidence: IDA GeneID:55829 -> Biological process: GO:0030970 [retrograde protein transport, ER to cytosol] evidence: IDA GeneID:55829 -> Biological process: GO:0032715 [negative regulation of interleukin-6 production] evidence: ISS GeneID:55829 -> Biological process: GO:0032720 [negative regulation of tumor necrosis factor production] evidence: ISS GeneID:55829 -> Biological process: GO:0032869 [cellular response to insulin stimulus] evidence: TAS GeneID:55829 -> Biological process: GO:0034599 [cellular response to oxidative stress] evidence: IMP GeneID:55829 -> Biological process: GO:0045184 [establishment of protein localization] evidence: TAS GeneID:55829 -> Biological process: GO:0045454 [cell redox homeostasis] evidence: IDA GeneID:55829 -> Biological process: GO:0045719 [negative regulation of glycogen biosynthetic process] evidence: TAS GeneID:55829 -> Biological process: GO:0046325 [negative regulation of glucose import] evidence: TAS GeneID:55829 -> Biological process: GO:0050728 [negative regulation of inflammatory response] evidence: IC GeneID:55829 -> Biological process: GO:0051771 [negative regulation of nitric-oxide synthase biosynthetic process] evidence: IMP GeneID:55829 -> Biological process: GO:0051775 [response to redox state] evidence: IDA GeneID:55829 -> Biological process: GO:0071222 [cellular response to lipopolysaccharide] evidence: IMP GeneID:55829 -> Biological process: GO:0080164 [regulation of nitric oxide metabolic process] evidence: IMP GeneID:55829 -> Biological process: GO:1902236 [negative regulation of intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress] evidence: IMP GeneID:55829 -> Biological process: GO:2000110 [negative regulation of macrophage apoptotic process] evidence: IMP GeneID:55829 -> Cellular component: GO:0005783 [endoplasmic reticulum] evidence: IDA GeneID:55829 -> Cellular component: GO:0005881 [cytoplasmic microtubule] evidence: IDA GeneID:55829 -> Cellular component: GO:0005886 [plasma membrane] evidence: TAS GeneID:55829 -> Cellular component: GO:0030176 [integral to endoplasmic reticulum membrane] evidence: IDA GeneID:55829 -> Cellular component: GO:0034361 [very-low-density lipoprotein particle] evidence: IDA GeneID:55829 -> Cellular component: GO:0034362 [low-density lipoprotein particle] evidence: IDA
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