INCA1
Protein INCA1
Also known as: INCA1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q0VD86
- Gene
- INCA1
- Ensembl
- ENSG00000196388
- Chromosome
- 17
- Canonical length
- 236 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
Enables cyclin binding activity; cyclin-dependent protein serine/threonine kinase inhibitor activity; and identical protein binding activity. Acts upstream of or within negative regulation of cyclin-dependent protein serine/threonine kinase activity. Located in cytoplasm and nuclear body. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
236 residues, UniProt reviewed canonical sequence.
>Q0VD86|INCA1
1 MQVQDDGVNL IPFAKCSRVV SRSPPPRLPS QSLRPMPQRY GDVFWKNLNQ RPTPTWLEEQ
61 HIPPMLRATG CSQLGLYPPE QLPPPEMLWR RKKRRPCLEG MQQQGLGGVP ARVRAVTYHL
121 EDLRRRQSII NELKKAQWGS SGAASEPVVL GEEGCGFPST NEYPDLEEER ATYPQEEDRF
181 LTPGRAQLLW SPWSPLDQEE ACASRQLHSL ASFSTVTARR NPLHNPWGME LAASEELocalizationUniProt · AlphaFold · HPA
Whether an antibody against INCA1 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)
- 0.66
- Highest tissue expression
- 46 nTPM
Expression across tissuesHPA
Tissue
- testis: 46 nTPM
- duodenum: 10 nTPM
- skeletal muscle: 10 nTPM
- lymph node: 8 nTPM
- skin: 7.4 nTPM
- thyroid gland: 7.4 nTPM
Single-cell type
- late spermatids: 513 nCPM
- early primary spermatocytes: 254 nCPM
- early spermatids: 122 nCPM
- late primary spermatocytes: 88 nCPM
- undifferentiated spermatogonia: 39 nCPM
- differentiating spermatogonia: 18 nCPM
Immune cell
- intermediate monocyte: 1.6 nTPM
- non-classical monocyte: 1.3 nTPM
- classical monocyte: 0.9 nTPM
- MAIT T-cell: 0.7 nTPM
- naive CD4 T-cell: 0.7 nTPM
- naive CD8 T-cell: 0.6 nTPM
Brain region
- pons: 15 nTPM
- cerebellum: 15 nTPM
- thalamus: 14 nTPM
- medulla oblongata: 14 nTPM
- white matter: 14 nTPM
- hypothalamus: 14 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)
- 1.8
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.23
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- none
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
- apoptotic signaling pathway
- fibroblast proliferation
- negative regulation of cell population proliferation
- negative regulation of cyclin-dependent protein serine/threonine kinase activity
- negative regulation of fibroblast proliferation
- positive regulation of apoptotic signaling pathway
Molecular functions
- cyclin binding
- cyclin-dependent protein serine/threonine kinase inhibitor activity
- identical protein binding
- protein-containing complex binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein INCA1
- INCA1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of INCA1 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 INCA1 as an antibody target. Whether an autoantibody or antibody against INCA1 could matter depends on whether native INCA1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
INCA1 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 INCA1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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