EXOSC1 (exosome component 1)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 51013 |
| Gene name | Exosome component 1 |
| Gene symbol | EXOSC1 |
| Synonyms (NCBI Gene) |
CGI-108CSL4Csl4pPCH1FSKI4Ski4pp13
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| Chromosome | 10 |
| Chromosome location | 10q24.1 |
| Summary | This gene encodes a core component of the exosome. The mammalian exosome is required for rapid degradation of AU rich element-containing RNAs but not for poly(A) shortening. The association of this protein with the exosome is mediated by protein-protein i |
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miRNA
miRNA information provided by mirtarbase database.
79
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
25
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q9Y3B2 | |||||||||||||||
| Protein name | Exosome complex component CSL4 (Exosome component 1) | |||||||||||||||
| Protein function | Non-catalytic component of the RNA exosome complex which has 3'->5' exoribonuclease activity and participates in a multitude of cellular RNA processing and degradation events. In the nucleus, the RNA exosome complex is involved in proper maturat | |||||||||||||||
| PDB | 2NN6 , 6D6Q , 6D6R , 6H25 , 9G8M , 9G8N , 9G8O , 9G8P | |||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 195 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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