SINHCAF
SIN3-HDAC complex-associated factor
Also known as: C12orf14, FAM60A, SHCAF_HUMAN, TERA
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NP50
- Gene
- SINHCAF
- Ensembl
- ENSG00000139146
- Chromosome
- 12
- Canonical length
- 221 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Involved in negative regulation of cell migration. Part of Sin3-type complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
221 residues, UniProt reviewed canonical sequence.
>Q9NP50|SINHCAF
1 MFGFHKPKMY RSIEGCCICR AKSSSSRFTD SKRYEKDFQS CFGLHETRSG DICNACVLLV
61 KRWKKLPAGS KKNWNHVVDA RAGPSLKTTL KPKKVKTLSG NRIKSNQISK LQKEFKRHNS
121 DAHSTTSSAS PAQSPCYSNQ SDDGSDTEMA SGSNRTPVFS FLDLTYWKRQ KICCGIIYKG
181 RFGEVLIDTH LFKPCCSNKK AAAEKPEEQG PEPLPISTQE WLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SINHCAF can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.54
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- endometrium: 49 nTPM
- thymus: 47 nTPM
- fallopian tube: 34 nTPM
- lymph node: 32 nTPM
- urinary bladder: 32 nTPM
- tonsil: 31 nTPM
Single-cell type
- choroid plexus epithelial cells: 170 nCPM
- early spermatids: 159 nCPM
- renal collecting duct intercalated cells: 129 nCPM
- fallopian secretory cells: 115 nCPM
- fallopian tube ciliated cells: 114 nCPM
- epididymal basal cells: 108 nCPM
Immune cell
- plasmacytoid DC: 72 nTPM
- memory B-cell: 59 nTPM
- NK-cell: 51 nTPM
- naive B-cell: 49 nTPM
- naive CD4 T-cell: 36 nTPM
- memory CD4 T-cell: 31 nTPM
Brain region
- choroid plexus: 22 nTPM
- cerebellum: 6.6 nTPM
- medulla oblongata: 5.3 nTPM
- basal ganglia: 5.1 nTPM
- midbrain: 4.2 nTPM
- spinal cord: 4.1 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.29
- gnomAD pLI
- 0.96
- DepMap mean gene effect
- -0.48
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of cell differentiation
- negative regulation of cell migration
- negative regulation of stem cell population maintenance
- negative regulation of transcription by RNA polymerase II
- negative regulation of transforming growth factor beta receptor signaling pathway
- positive regulation of cell population proliferation
- positive regulation of stem cell population maintenance
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SIN3-HDAC complex-associated factor
- Protein Family FAM60A
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SINHCAF in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SINHCAF as an antibody target. Whether an autoantibody or antibody against SINHCAF could matter depends on whether native SINHCAF is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SINHCAF is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SINHCAF as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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