CHCHD10

From Infogalactic: the planetary knowledge core
Jump to: navigation, search

CHCHD10, whose full official name is coiled-coil-helix-coiled-coil-helix domain containing 10, is a gene found in Humans encoding a mitochondrial 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 mitochondrial myopathy,[1] amyotrophic lateral sclerosis (ALS),[2] frontotemporal dementia (FTD),[2] late-onset spinal motor neuronopathy (SMAJ), and cerebellar ataxia. Alternative splicing of this gene results in multiple transcript variants.

References

  1. Lua error in package.lua at line 80: module 'strict' not found.
  2. 2.0 2.1 Lua error in package.lua at line 80: module 'strict' not found.

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

<templatestyles src="Asbox/styles.css"></templatestyles>