SIN3B (SIN3 transcription regulator family member B)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 23309 |
| Gene name | SIN3 transcription regulator family member B |
| Gene symbol | SIN3B |
| Synonyms (NCBI Gene) |
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| Chromosome | 19 |
| Chromosome location | 19p13.11 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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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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O75182 | |||||||||||||||||||||||||||||||||||
| Protein name | Paired amphipathic helix protein Sin3b (Histone deacetylase complex subunit Sin3b) (Transcriptional corepressor Sin3b) | |||||||||||||||||||||||||||||||||||
| Protein function | Acts as a transcriptional repressor. Interacts with MXI1 to repress MYC responsive genes and antagonize MYC oncogenic activities. Interacts with MAD-MAX heterodimers by binding to MAD. The heterodimer then represses transcription by tethering SI | |||||||||||||||||||||||||||||||||||
| PDB | 8BPA , 8BPB , 8BPC , 8C60 | |||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence | ||||||||||||||||||||||||||||||||||||
| Sequence length | 1162 | |||||||||||||||||||||||||||||||||||
| 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.).
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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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