Gene Symbol | SLC25A46 |
Entrez Gene ID | 91137 |
Full Name | solute carrier family 25 member 46 |
Synonyms | HMSN6B |
General protein information |
|
Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Summary | This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016]. |
Disorder MIM: | |
Disorder Html: | Neuropathy, hereditary motor and sensory, type VIB, 616505 (3) |