CENPO
Centromere protein O
Also known as: CENP-O, CENPO_HUMAN, MGC11266
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BU64
- Gene
- CENPO
- Ensembl
- ENSG00000138092
- Chromosome
- 2
- Canonical length
- 300 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
This gene encodes a component of the interphase centromere complex. The encoded protein is localized to the centromere throughout the cell cycle and is required for bipolar spindle assembly, chromosome segregation and checkpoint signaling during mitosis. Alternatively spliced transcript variants encoding multiple protein isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]
Canonical amino-acid sequenceUniProt
300 residues, UniProt reviewed canonical sequence.
>Q9BU64|CENPO
1 MEQANPLRPD GESKGGVLAH LERLETQVSR SRKQSEELQS VQAQEGALGT KIHKLRRLRD
61 ELRAVVRHRR ASVKACIANV EPNQTVEINE QEALEEKLEN VKAILQAYHF TGLSGKLTSR
121 GVCVCISTAF EGNLLDSYFV DLVIQKPLRI HHHSVPVFIP LEEIAAKYLQ TNIQHFLFSL
181 CEYLNAYSGR KYQADRLQSD FAALLTGPLQ RNPLCNLLSF TYKLDPGGQS FPFCARLLYK
241 DLTATLPTDV TVTCQGVEVL STSWEEQRAS HETLFCTKPL HQVFASFTRK GEKLDMSLVSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CENPO 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)
- 0.39
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- thymus: 11 nTPM
- bone marrow: 8.7 nTPM
- testis: 8.1 nTPM
- tonsil: 5.5 nTPM
- adipose tissue: 5 nTPM
- cerebral cortex: 4.7 nTPM
Single-cell type
- epicardial cells: 39 nCPM
- erythrocyte progenitors: 38 nCPM
- pericytes: 34 nCPM
- monocyte progenitors: 31 nCPM
- differentiating spermatogonia: 30 nCPM
- extravillous trophoblasts: 29 nCPM
Immune cell
- plasmacytoid DC: 1.1 nTPM
- gdT-cell: 1 nTPM
- naive CD8 T-cell: 0.7 nTPM
- NK-cell: 0.7 nTPM
- T-reg: 0.7 nTPM
- memory CD8 T-cell: 0.5 nTPM
Brain region
- hypothalamus: 7.8 nTPM
- medulla oblongata: 7.7 nTPM
- hippocampal formation: 7.6 nTPM
- pons: 7.3 nTPM
- amygdala: 7.1 nTPM
- cerebral cortex: 7.1 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)
- 1.3
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.4
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
- cytosol
- inner kinetochore
- nuclear body
- nucleoplasm
- nucleus
- Mis6-Sim4 complex
Protein domainsUniProt · Pfam · InterPro
- Centromere protein O
- Cenp-O kinetochore centromere component
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CENPO 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 CENPO as an antibody target. Whether an autoantibody or antibody against CENPO could matter depends on whether native CENPO is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CENPO 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 CENPO as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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