CETN3
Centrin-3
Also known as: CEN3, CETN3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15182
- Gene
- CETN3
- Ensembl
- ENSG00000153140
- Chromosome
- 5
- Canonical length
- 167 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Centrosome,Basal body
OverviewNCBI Gene
The protein encoded by this gene contains four EF-hand calcium binding domains, and is a member of the centrin protein family. Centrins are evolutionarily conserved proteins similar to the CDC31 protein of S. cerevisiae. Yeast CDC31 is located at the centrosome of interphase and mitotic cells, where it plays a fundamental role in centrosome duplication and separation. Multiple forms of the proteins similar to the yeast centrin have been identified in human and other mammalian cells, some of which have been shown to be associated with centrosome fractions. This protein appears to be one of the most abundant centrins associated with centrosome, which suggests a similar function to its yeast counterpart. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]
Canonical amino-acid sequenceUniProt
167 residues, UniProt reviewed canonical sequence.
>O15182|CETN3
1 MSLALRSELV VDKTKRKKRR ELSEEQKQEI KDAFELFDTD KDEAIDYHEL KVAMRALGFD
61 VKKADVLKIL KDYDREATGK ITFEDFNEVV TDWILERDPH EEILKAFKLF DDDDSGKISL
121 RNLRRVAREL GENMSDEELR AMIEEFDKDG DGEINQEEFI AIMTGDILocalizationUniProt · AlphaFold · HPA
Whether an antibody against CETN3 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)
- 0.35
- Highest tissue expression
- 122 nTPM
Expression across tissuesHPA
Tissue
- testis: 122 nTPM
- retina: 33 nTPM
- ovary: 29 nTPM
- choroid plexus: 26 nTPM
- parathyroid gland: 23 nTPM
- breast: 23 nTPM
Single-cell type
- late primary spermatocytes: 969 nCPM
- early primary spermatocytes: 322 nCPM
- extravillous trophoblasts: 86 nCPM
- megakaryocytes: 80 nCPM
- cytotrophoblasts: 77 nCPM
- esophageal apical cells: 77 nCPM
Immune cell
- plasmacytoid DC: 31 nTPM
- memory B-cell: 27 nTPM
- naive B-cell: 22 nTPM
- naive CD4 T-cell: 21 nTPM
- basophil: 20 nTPM
- NK-cell: 17 nTPM
Brain region
- white matter: 34 nTPM
- medulla oblongata: 23 nTPM
- basal ganglia: 21 nTPM
- hypothalamus: 20 nTPM
- midbrain: 20 nTPM
- thalamus: 20 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)
- 1.41
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.39
- DepMap mean gene effect
- -0.03
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CETN3 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 CETN3 as an antibody target. Whether an autoantibody or antibody against CETN3 could matter depends on whether native CETN3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CETN3 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 CETN3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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