CHCHD10

CHCHD10, whose full official name is coiled-coil-helix-coiled-coil-helix domain containing 10, is a gene found in Humans encoding a protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. CHCHD10-related disorders include ,amyotrophic lateral sclerosis (ALS),frontotemporal dementia (FTD),late-onset spinal motor neuronopathy (SMAJ), and cerebellar ataxia. Alternative splicing of this gene results in multiple transcript variants.

This article incorporates text from the United States National Library of Medicine ([1]), which is in the public domain.