COTL1
Coactosin-like protein
Also known as: CLP, COTL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14019
- Gene
- COTL1
- Ensembl
- ENSG00000103187
- Chromosome
- 16
- Canonical length
- 142 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes one of the numerous actin-binding proteins which regulate the actin cytoskeleton. This protein binds F-actin, and also interacts with 5-lipoxygenase, which is the first committed enzyme in leukotriene biosynthesis. Although this gene has been reported to map to chromosome 17 in the Smith-Magenis syndrome region, the best alignments for this gene are to chromosome 16. The Smith-Magenis syndrome region is the site of two related pseudogenes. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
142 residues, UniProt reviewed canonical sequence.
>Q14019|COTL1
1 MATKIDKEAC RAAYNLVRDD GSAVIWVTFK YDGSTIVPGE QGAEYQHFIQ QCTDDVRLFA
61 FVRFTTGDAM SKRSKFALIT WIGENVSGLQ RAKTGTDKTL VKEVVQNFAK EFVISDRKEL
121 EEDFIKSELK KAGGANYDAQ TELocalizationUniProt · AlphaFold · HPA
Whether an antibody against COTL1 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)
- 0.32
- Highest tissue expression
- 350 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 350 nTPM
- spleen: 315 nTPM
- appendix: 279 nTPM
- bone marrow: 258 nTPM
- tonsil: 247 nTPM
- kidney: 145 nTPM
Single-cell type
- extravillous trophoblasts: 2,134 nCPM
- neutrophils: 1,408 nCPM
- monocytes: 1,347 nCPM
- cdc: 1,072 nCPM
- kupffer cells: 979 nCPM
- platelets: 979 nCPM
Immune cell
- non-classical monocyte: 4,601 nTPM
- intermediate monocyte: 4,072 nTPM
- eosinophil: 3,426 nTPM
- total PBMC: 2,951 nTPM
- classical monocyte: 2,442 nTPM
- myeloid DC: 2,397 nTPM
Brain region
- thalamus: 169 nTPM
- medulla oblongata: 134 nTPM
- white matter: 131 nTPM
- pons: 128 nTPM
- hypothalamus: 124 nTPM
- basal ganglia: 119 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about COTL1.
Disease | ImmuneIEDB
Conditions an epitope on COTL1 was assayed in.
- skin melanoma 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)
- 1.18
- gnomAD pLI
- 0.04
- gnomAD missense Z
- -0.13
- DepMap mean gene effect
- 0
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of COTL1 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 COTL1 as an antibody target. Whether an autoantibody or antibody against COTL1 could matter depends on whether native COTL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COTL1 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 COTL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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