Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
58516
Gene name Gene Name - the full gene name approved by the HGNC.
SIN3-HDAC complex associated factor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SINHCAF
Synonyms (NCBI Gene) Gene synonyms aliases
C12orf14, FAM60A, L4, TERA
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12p11.21
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT703663 hsa-miR-495-5p HITS-CLIP 23313552
MIRT703662 hsa-miR-34b-3p HITS-CLIP 23313552
MIRT703661 hsa-miR-6808-5p HITS-CLIP 23313552
MIRT703660 hsa-miR-6893-5p HITS-CLIP 23313552
MIRT703659 hsa-miR-940 HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II NAS 22865885
GO:0005515 Function Protein binding IPI 23752268, 26496610, 28514442, 32296183, 33961781, 35271311
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus NAS 28554894
GO:0008284 Process Positive regulation of cell population proliferation IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615027 30702 ENSG00000139146
Protein
UniProt ID Q9NP50
Protein name SIN3-HDAC complex-associated factor (Protein FAM60A) (Tera protein homolog)
Protein function Subunit of the Sin3 deacetylase complex (Sin3/HDAC), this subunit is important for the repression of genes encoding components of the TGF-beta signaling pathway (PubMed:22865885, PubMed:22984288). Core component of a SIN3A complex (composed of a
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15396 FAM60A 2 198 Protein Family FAM60A Family
Sequence
Sequence length 221
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Coronary artery disease Coronary artery disease N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Esophageal Neoplasms Associate 28169357
Osteosarcoma Stimulate 37439040