Seroatlas · Human Serome Atlas

CENPW

Centromere protein W

Also known as: C6orf173, CENPW_HUMAN, CUG2

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q5EE01
Gene
CENPW
Ensembl
ENSG00000203760
Chromosome
6
Canonical length
88 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nucleoplasm

OverviewNCBI Gene

Predicted to enable DNA binding activity and protein heterodimerization activity. Involved in chromosome segregation; kinetochore assembly; and mitotic cell cycle. Located in kinetochore and nucleoplasm. Part of inner kinetochore. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

88 residues, UniProt reviewed canonical sequence.

>Q5EE01|CENPW
     1  MALSTIVSQR KQIKRKAPRG FLKRVFKRKK PQLRLEKSGD LLVHLNCLLF VHRLAEESRT
    61  NACASKCRVI NKEHVLAAAK VILKKSRG

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CENPW 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)
0.49
Highest tissue expression
48 nTPM

Expression across tissuesHPA

Tissue

  • bone marrow: 48 nTPM
  • testis: 37 nTPM
  • thymus: 25 nTPM
  • esophagus: 23 nTPM
  • tonsil: 19 nTPM
  • endometrium: 18 nTPM

Single-cell type

  • late primary spermatocytes: 499 nCPM
  • gastric progenitor cells: 277 nCPM
  • esophageal basal cells: 259 nCPM
  • early spermatids: 243 nCPM
  • extravillous trophoblasts: 183 nCPM
  • submucosal glandular cells: 122 nCPM

Immune cell

  • intermediate monocyte: 20 nTPM
  • plasmacytoid DC: 19 nTPM
  • classical monocyte: 17 nTPM
  • myeloid DC: 16 nTPM
  • non-classical monocyte: 14 nTPM
  • T-reg: 12 nTPM

Brain region

  • hippocampal formation: 7.3 nTPM
  • cerebral cortex: 6 nTPM
  • basal ganglia: 3.7 nTPM
  • white matter: 3.5 nTPM
  • amygdala: 2.8 nTPM
  • hypothalamus: 2.8 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)
0.93
gnomAD pLI
0.41
gnomAD missense Z
0.75
DepMap mean gene effect
-1.66
DepMap dependency class
pan

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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

  • Histone-fold
  • Centromere protein W
  • Centromere Protein W/WIP1
  • CENP-W protein

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of CENPW 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 CENPW as an antibody target. Whether an autoantibody or antibody against CENPW could matter depends on whether native CENPW is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CENPW 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 CENPW as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CENPW. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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