C2CD4A
C2 calcium-dependent domain-containing protein 4A
Also known as: C2C4A_HUMAN, FAM148A, NLF1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NCU7
- Gene
- C2CD4A
- Ensembl
- ENSG00000198535
- Chromosome
- 15
- Canonical length
- 369 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
Involved in positive regulation of acute inflammatory response; regulation of cell adhesion; and regulation of vascular permeability involved in acute inflammatory response. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
369 residues, UniProt reviewed canonical sequence.
>Q8NCU7|C2CD4A
1 MWCLERLRLG PECLRRSGDW LLPGRARGAK SRTTAACANV LTPDRIPEFC IPPRLMPRLA
61 LAALRNSWVE EAGMDEGAGR TDWDPRSQAA LSLPHLPRVR TAYGFCALLE SPHTRRKESL
121 LLGGPPAPRP RAHTYGGGGG PDALLGTLRV PRAPGPATPA APGCPRPPQD ALARRPRGCR
181 LLRVPDGLLS RALRAGRSRR LTRVRSVSSG NEDKERRAGS QSPARAPSTS PPSSRVPFPE
241 RLEAEGTVAL GRAGDALRLA AEYCPGTGRL RLRLLRAESP AGGAPGPRAV SCRLSLVLRP
301 PGTALRQCST VVGRSRKASF DQDFCFDGLS EDEVRRLAVR VKARDEGRGR ERGRLLGQGE
361 LSLGALLLLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against C2CD4A 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)
- 0.57
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 13 nTPM
- pancreas: 3.8 nTPM
- urinary bladder: 3.4 nTPM
- liver: 2.2 nTPM
- kidney: 2.1 nTPM
- stomach: 2 nTPM
Single-cell type
- pancreatic islet cells: 243 nCPM
- endometrial glandular cells: 194 nCPM
- ocular epithelial cells: 36 nCPM
- medullary thymic epithelial cells: 34 nCPM
- endometrial luminal cells: 24 nCPM
- endometrial secretory cells: 23 nCPM
Immune cell
- neutrophil: 0.3 nTPM
- basophil: 0.2 nTPM
- T-reg: 0.2 nTPM
- naive B-cell: 0.1 nTPM
- NK-cell: 0.1 nTPM
- plasmacytoid DC: 0.1 nTPM
Brain region
- hypothalamus: 6.5 nTPM
- cerebral cortex: 5.6 nTPM
- medulla oblongata: 3.4 nTPM
- midbrain: 3 nTPM
- pons: 2.7 nTPM
- choroid plexus: 1.8 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about C2CD4A.
Disease | ImmuneIEDB
Conditions an epitope on C2CD4A was assayed in.
- colonic benign neoplasm T cell
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)
- 1.55
- gnomAD pLI
- 0.02
- gnomAD missense Z
- -0.25
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- positive regulation of acute inflammatory response
- regulation of cell adhesion
- regulation of vascular permeability involved in acute inflammatory response
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads C2CD4A as an antibody target. Whether an autoantibody or antibody against C2CD4A could matter depends on whether native C2CD4A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
C2CD4A 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 C2CD4A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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