COLCA1
Colorectal cancer-associated protein 1
Also known as: COLC1_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for COLCA1 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
124 residues, UniProt reviewed canonical sequence.
>Q6ZS62|COLCA1
1 MESCSVAQAG VLTSPFMWRW TGMAGALSAL DNTIEDDADD QLPCGEGRPG WVRGELLGSQ
61 GVCKDSKDLF VPTSSSLYGC FCVGLVSGMA ISVLLLASDF RKLDFSRPEP CFEKEASLWF
121 VAQHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COLCA1 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
- 1
- Mean surface accessibility (rSASA)
- 0.63
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 missense Z
- -0.17
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
Cellular components
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads COLCA1 as an antibody target. Whether an autoantibody or antibody against COLCA1 could matter depends on whether native COLCA1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COLCA1 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 COLCA1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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