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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A46-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| SLC25A46-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| SLC25A46-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| SLC25A46-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| SLC25A46-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
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]
Gene Symbol : SLC25A46
Gene Name : Solute carrier family 25 member 46
Chromosome : CHR 5: 110,738,135-110,765,160
Locus : 5q22.1
Alt. Genes : FEM1B
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.