SLC25A46 solute carrier family 25 member 46 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 91137)
Source: NCBI Gene (ID 91137)
Symbol: SLC25A46
Full name: solute carrier family 25 member 46
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: HMSN6B; PCH1E
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]
Expression: Ubiquitous expression in brain (RPKM 17.7), thyroid (RPKM 13.2) and 25 other tissues
Orthologs: mouse
Gene size: 27013bp
Exon count: 10