CCDC125
Coiled-coil domain-containing protein 125
Also known as: CC125_HUMAN, KENAE
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86Z20
- Gene
- CCDC125
- Ensembl
- ENSG00000183323
- Chromosome
- 5
- Canonical length
- 511 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear membrane,Intermediate filaments
OverviewNCBI Gene
Enables identical protein binding activity. Involved in activation of GTPase activity; negative regulation of Rho protein signal transduction; and negative regulation of cell motility. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
511 residues, UniProt reviewed canonical sequence.
>Q86Z20|CCDC125
1 MSKVARSSSE SDVQLWETEE DDMTEGDLGY GLGRKPGGIY EIEFSHRSRK RSDGKNFSPP
61 PFPRKGEERN EASFQYSKHK SQQDTFPQVS RISNYRRQSS TVDSNSELSN EELRQCLNET
121 LEEVEMLKTE LEASQRQLRG KEEALKILQS MAILGKATSH TQAVLQKTME QNRSLEKEIN
181 ALQWEIEFDH NRFKNIEESW IQKYDRLNCE NAVLKENLKV KTEEIKMLKS DNAVLNQRYL
241 EALAMLDIKQ QKMAQENMCC DKSGFAEASG LELAVLGACL CHGPGGNPCS CARMAASTRK
301 LLLQLKQELE ILQKSKEEAY VMADAFRIAF EQQLMRKNDQ ALQLTQMDKM HKKATKWMNW
361 KHLKEDGFPS PRSKKTFGQR LLGMLPSENS SKRMEDQDSP QEVLKMLIDL LNDKEEALAH
421 QRKVSYMLAR ALEDKDTASN ENKEKNPIKE NFPFNNPWRK TSEFSVLGDP IHSSVCILNS
481 VGCICSIQHS QIDPNYRTLK RSHSLPSSII FLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCDC125 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)
- 0.57
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- liver: 12 nTPM
- bone marrow: 10 nTPM
- breast: 6.5 nTPM
- prostate: 6.5 nTPM
- salivary gland: 6.2 nTPM
- stomach: 5.5 nTPM
Single-cell type
- neutrophil progenitors: 74 nCPM
- distal convoluted tubule cells: 67 nCPM
- microglia: 63 nCPM
- choroid plexus epithelial cells: 61 nCPM
- renal connecting tubule cells: 59 nCPM
- papillary tip epithelial cells: 58 nCPM
Immune cell
- eosinophil: 15 nTPM
- neutrophil: 11 nTPM
- basophil: 7 nTPM
- non-classical monocyte: 2.8 nTPM
- myeloid DC: 1.6 nTPM
- plasmacytoid DC: 1.3 nTPM
Brain region
- white matter: 7.8 nTPM
- medulla oblongata: 7.4 nTPM
- choroid plexus: 6.6 nTPM
- midbrain: 6.6 nTPM
- cerebral cortex: 6.3 nTPM
- pons: 6.3 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)
- 1.03
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.35
- DepMap mean gene effect
- -0.11
- 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
- activation of GTPase activity
- negative regulation of cell motility
- negative regulation of Rho protein signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Coiled-coil domain-containing protein 125
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CCDC125 as an antibody target. Whether an autoantibody or antibody against CCDC125 could matter depends on whether native CCDC125 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCDC125 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 CCDC125 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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