CHORDC1
Cysteine and histidine-rich domain-containing protein 1
Also known as: CHP-1, CHP1, CHRD1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UHD1
- Gene
- CHORDC1
- Ensembl
- ENSG00000110172
- Chromosome
- 11
- Canonical length
- 332 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Enables Hsp90 protein binding activity. Predicted to be involved in several processes, including centrosome duplication; chaperone-mediated protein folding; and negative regulation of Rho-dependent protein serine/threonine kinase activity. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
332 residues, UniProt reviewed canonical sequence.
>Q9UHD1|CHORDC1
1 MALLCYNRGC GQRFDPETNS DDACTYHPGV PVFHDALKGW SCCKRRTTDF SDFLSIVGCT
61 KGRHNSEKPP EPVKPEVKTT EKKELCELKP KFQEHIIQAP KPVEAIKRPS PDEPMTNLEL
121 KISASLKQAL DKLKLSSGNE ENKKEEDNDE IKIGTSCKNG GCSKTYQGLE SLEEVCVYHS
181 GVPIFHEGMK YWSCCRRKTS DFNTFLAQEG CTKGKHMWTK KDAGKKVVPC RHDWHQTGGE
241 VTISVYAKNS LPELSRVEAN STLLNVHIVF EGEKEFDQNV KLWGVIDVKR SYVTMTATKI
301 EITMRKAEPM QWASLELPAA KKQEKQKDAT TDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CHORDC1 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 26 nTPM
- hypothalamus: 26 nTPM
- ovary: 26 nTPM
- hippocampal formation: 24 nTPM
- cerebral cortex: 23 nTPM
- midbrain: 23 nTPM
Single-cell type
- ependymal cells: 118 nCPM
- early spermatids: 82 nCPM
- choroid plexus epithelial cells: 74 nCPM
- oligodendrocytes: 67 nCPM
- other brain neurons: 60 nCPM
- late spermatids: 57 nCPM
Immune cell
- T-reg: 18 nTPM
- NK-cell: 17 nTPM
- intermediate monocyte: 14 nTPM
- naive CD4 T-cell: 14 nTPM
- naive CD8 T-cell: 13 nTPM
- MAIT T-cell: 13 nTPM
Brain region
- white matter: 34 nTPM
- cerebral cortex: 23 nTPM
- hypothalamus: 23 nTPM
- hippocampal formation: 21 nTPM
- medulla oblongata: 20 nTPM
- pons: 19 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)
- 0.38
- gnomAD pLI
- 0.9
- gnomAD missense Z
- 0.74
- DepMap mean gene effect
- -0.73
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- centrosome duplication
- protein folding
- regulation of cellular response to heat
- regulation of centrosome duplication
Molecular functions
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CHORDC1 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 CHORDC1 as an antibody target. Whether an autoantibody or antibody against CHORDC1 could matter depends on whether native CHORDC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CHORDC1 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 CHORDC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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