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Pathways
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16 records found for search term Exosc3
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1304739Exosc3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN CUT catabolic process (ortholog); DNA deamination (ortholog); isotype switching (ortholog); PARTICIPATES IN RNA degradation pathway; ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence sy56436949564374711Rat114symbol , PhenoGengene, protein-coding, VALIDATED [RefSeq]
1312357EXOSC3exosome component 3This gene encodes a non-catalytic component of the human exosome, a complex with 3'-5' exoribonuclease activity that plays a role in numerous RNA processing and degradation activities. Related pseudogenes of this gene are found on chromosome 19 and 21. Alternatively spliced transcript variants encod93777971437785092Human214symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1312358Exosc3exosome component 3Predicted to enable RNA binding activity. Involved in isotype switching. Acts upstream of or within positive regulation of isotype switching. Predicted to be located in cytosol; euchromatin; and nuclear lumen. Predicted to be part of cytoplasmic exosome (RNase complex) and nuclear exosome (RNase com44531661345320616Mouse152symbol , PhenoGen , descriptiongene, protein-coding, VALIDATED [RefSeq]
8733326Exosc3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN CUT catabolic process (ortholog); DNA deamination (ortholog); isotype switching (ortholog); ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortNW_0049554192868389628692006Chinchilla44symbolgene, protein-coding, MODEL [RefSeq]
11677279EXOSC3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN positive regulation of isotype switching (ortholog); ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (inferred); 93761117337634869Bonobo64symbolgene, protein-coding, MODEL [RefSeq]
12325976EXOSC3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN positive regulation of isotype switching (ortholog); ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (inferred); 115407299354079024Dog64symbolgene, protein-coding, MODEL [RefSeq]
12678558Exosc3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN positive regulation of isotype switching (ortholog); ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (inferred); NW_00493652455808555586170Squirrel64symbolgene, protein-coding, MODEL [RefSeq]
155258170exosc3Tropical Clawed Frogsymbolgene, null
14155872EXOSC3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN positive regulation of isotype switching (ortholog); ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (inferred); Pig65symbolgene, protein-coding, MODEL [RefSeq]
626098825Exosc3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN CUT catabolic process (ortholog); DNA deamination (ortholog); isotype switching (ortholog); ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortBlack Rat44symbolgene, protein-coding, MODEL [RefSeq]
18414388EXOSC3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN positive regulation of isotype switching (ortholog); ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (inferred); Green Monkey64symbolgene, protein-coding, MODEL [RefSeq]
18932094Exosc3exosome component 3ENCODES a protein that exhibits RNA exonuclease activity (ortholog); INVOLVED IN positive regulation of isotype switching (ortholog); ASSOCIATED WITH congenital myopathy (ortholog); fetal akinesia deformation sequence syndrome 1 (ortholog); genetic disease (ortholog); FOUND IN cytoplasm (inferred); Naked Mole-Rat65symbolgene, protein-coding, MODEL [RefSeq]
155258171exosc3.LAfrican Clawed Frogsymbolgene, null
16567807AL161423.1exosome component 3 (EXOSC3)Humannamegene, unprocessed_pseudogene
2293248EXOSC3P1exosome component 3 pseudogene 1213249681232497568Humansymbol , COSMIC , Human Proteome Mapgene, pseudo, INFERRED [RefSeq]
2301482EXOSC3P2exosome component 3 pseudogene 21978127177814428Humansymbol , COSMIC , Human Proteome Mapgene, pseudo, INFERRED [RefSeq]