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Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial (CHCHD10)

Homo sapiens — UniProt Q8WYQ3

Gene: CHCHD10Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial (CHCHD10) is a protein from Homo sapiens identified by UniProt accession Q8WYQ3, 142 residues long. MolForge cross-references it against 0 known binders and 187 disease associations.

  • UniProt accession: Q8WYQ3; gene symbol CHCHD10.
  • Organism: Homo sapiens.
  • Length: 142 amino acids.
  • Top disease associations (Open Targets): lower motor neuron syndrome with late-adult onset, frontotemporal dementia with motor neuron disease and autosomal dominant mitochondrial myopathy with exercise intolerance.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameCoiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
UniProt accessionQ8WYQ3
GeneCHCHD10
OrganismHomo sapiens
Length142 residues
Molecular weight—
EC numbers—
Target class—
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (187)

Diseases linked to this target (Open Targets).

  • lower motor neuron syndrome with late-adult onset · score 0.74
  • frontotemporal dementia with motor neuron disease · score 0.72
  • autosomal dominant mitochondrial myopathy with exercise intolerance · score 0.70
  • Mitochondrial myopathy · score 0.53
  • amyotrophic lateral sclerosis · score 0.40
  • Amyotrophic lateral sclerosis · score 0.37
  • mitochondrial disease · score 0.37
  • serum IgG glycosylation measurement · score 0.35
  • erythrocyte count · score 0.22
  • lymphocyte count · score 0.20

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8WYQ3-F1alphafoldPREDICTED61.42—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q8WYQ3.

Amino-acid sequence (142 residues)

MPRGSRSAAS RPASRPAAPS AHPPAHPPPS AAAPAPAPSG QPGLMAQMAT TAAGVAVGSA VGHVMGSALT GAFSGGSSEP SQPAVQQAPT PAAPQPLQMG PCAYEIRQFL DCSTTQSDLS LCEGFSEALK QCKYYHGLSS LP

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with CHCHD10?

The strongest Open Targets associations for CHCHD10 are lower motor neuron syndrome with late-adult onset, frontotemporal dementia with motor neuron disease, autosomal dominant mitochondrial myopathy with exercise intolerance, Mitochondrial myopathy and amyotrophic lateral sclerosis.

How long is the CHCHD10 protein?

The Homo sapiens CHCHD10 protein (UniProt Q8WYQ3) is 142 amino acids long.

Browse: Targets: C · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ8WYQ3
GeneCHCHD10
OrganismHomo sapiens
Length142
Binders0
Diseases187
View on UniProt