CHCHD2 Chromosome 7
Coiled-coil-helix-coiled-coil-helix domain containing 2
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What This Gene Does
The protein encoded by this gene belongs to a class of eukaryotic CX(9)C proteins characterized by four cysteine residues spaced ten amino acids apart from one another. These residues form disulfide linkages that define a CHCH fold. In response to stress, the protein translocates from the mitochondrial intermembrane space to the nucleus where it binds to a highly conserved 13 nucleotide oxygen responsive element in the promoter of cytochrome oxidase 4I2, a subunit of the terminal enzyme of the electron transport chain. In concert with recombination signal sequence-binding protein J, binding of this protein activates the oxygen responsive element at four percent oxygen. In addition, it has been shown that this protein is a negative regulator of mitochondria-mediated apoptosis. In response to apoptotic stimuli, mitochondrial levels of this protein decrease, allowing BCL2-associated X protein to oligomerize and activate the caspase cascade. Pseudogenes of this gene are found on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Gene Info
Gene Group
Coiled-coil-helix-coiled-coil-helix domain containing proteins
Locus Type
gene with protein product
Location
7p11.2
Ensembl
ENSG00000106153
Associated Conditions (2)
Parkinson disease 22
autosomal dominant
Key Variants
All Variants (3)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS757126911 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS750014782 | Health Risk | Pathogenic | Parkinson disease 22, autosomal dominant, Parkinson disease 22 |
| RS864309650 | Health Risk | Pathogenic | Parkinson disease 22, autosomal dominant, Parkinson disease 22 |