Slc25a46 - solute carrier family 25, member 46 Gene
Also Known as RGD1305072
Species: Rattus norvegicus
Gene Type: protein coding
Gene ID: 291709
Summary
Predicted to be involved in axon development and mitochondrial membrane fission. Predicted to act upstream of or within several processes, including Autophagy of mitochondrion; locomotion involved in locomotory behavior; and nervous system development. Predicted to be located in mitochondrion. Predicted to be active in mitochondrial outer membrane. Human ortholog(s) of this gene implicated in pontocerebellar hypoplasia. Orthologous to human SLC25A46 (solute carrier family 25 member 46). [provided by Alliance of Genome Resources, Apr 2022]
Slc25a46 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001100515.1 | NP_001093985.1 | mitochondrial outer membrane protein SLC25A46 |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
mitochondrial outer membrane protein SLC25A46 solute carrier family 25 member 46 |
|
|
Related Agents
- Pre-clinical Phase
Pre-clinical Phase
Bioactive Molecules
(1)
| Cat. No. | Product Name |
Effect
|
Purity |
Rare Diseases
|
|---|---|---|---|---|
| HY-RS13128 | SLC25A46 Human Pre-designed siRNA Set A | Pre-designed Set | / | Unkown |
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