ARID3C
AT-rich interactive domain-containing protein 3C
Also known as: ARI3C_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NKF2
- Gene
- ARID3C
- Ensembl
- ENSG00000205143
- Chromosome
- 9
- Canonical length
- 412 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
OverviewNCBI Gene
This gene is a member of the ARID (AT-rich interaction domain) family of proteins. The ARID domain is a helix-turn-helix motif-based DNA-binding domain. ARID family members have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
412 residues, UniProt reviewed canonical sequence.
>A6NKF2|ARID3C
1 MEALQKQQAA RLAQGVGPLA PACPLLPPQP PLPDHRTLQA PEGALGNVGA EEEEDAEEDE
61 EKREEAGAEE EAAEESRPGA QGPSSPSSQP PGLHPHEWTY EEQFKQLYEL DADPKRKEFL
121 DDLFSFMQKR GTPVNRVPIM AKQVLDLYAL FRLVTAKGGL VEVINRKVWR EVTRGLSLPT
181 TITSAAFTLR TQYMKYLYPY ECETRALSSP GELQAAIDSN RREGRRQAYT ATPLFGLAGP
241 PPRGAQDPAL GPGPAPPATQ SSPGPAQGST SGLPAHACAQ LSPSPIKKEE SGIPNPCLAL
301 PVGLALGPTR EKLAPEEPPE KRAVLMGPMD PPRPCMPPSF LPRGKVPLRE ERLDGPLNLA
361 GSGISSINMA LEINGVVYTG VLFARRQPVP ASQGPTNPAP PPSTGPPSSI LPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARID3C 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)
- 0.59
- Highest tissue expression
- 10 nTPM
Expression across tissuesHPA
Tissue
- liver: 10 nTPM
- cerebral cortex: 0.3 nTPM
- skin: 0.3 nTPM
- testis: 0.3 nTPM
- cerebellum: 0.2 nTPM
- fallopian tube: 0.2 nTPM
Single-cell type
- hepatocytes: 4.3 nCPM
- gastric progenitor cells: 1.3 nCPM
- late spermatids: 0.8 nCPM
- retinal amacrine cells: 0.7 nCPM
- basal prostatic cells: 0.6 nCPM
- early spermatids: 0.5 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- pons: 3.4 nTPM
- cerebral cortex: 2.6 nTPM
- hypothalamus: 2.4 nTPM
- medulla oblongata: 2.3 nTPM
- white matter: 1.7 nTPM
- cerebellum: 1.5 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)
- 1.4
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.49
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- macrophage differentiation
- positive regulation of transcription by RNA polymerase II
- regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARID3C 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 ARID3C as an antibody target. Whether an autoantibody or antibody against ARID3C could matter depends on whether native ARID3C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARID3C 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 ARID3C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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