{"symbol":"SLC25A46","synonyms":["HMSN6B"],"name":"solute carrier family 25, member 46","description":"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]","ncbiEntrezGeneId":91137,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/91137","proteins":[{"symbol":"S2546_HUMAN","href":"/api/1.0/protein/S2546_HUMAN"}],"hgncRootFamilies":[{"name":"Solute carriers (SLC)","href":"/api/1.0/gene_family/Solute+carriers+%28SLC%29"}]}