CHCHD2 Chromosome 7

Coiled-coil-helix-coiled-coil-helix domain containing 2
3 variants 3 Health Risk

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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
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