Gene
slc25a46
- ID
- ZDB-GENE-040718-296
- Name
- solute carrier family 25 member 46
- Symbol
- slc25a46 Nomenclature History
- Previous Names
-
- zgc:92767
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Involved in axon development and mitochondrial fission. Localizes to neuron projection. Is expressed in brain and eye. Orthologous to human SLC25A46 (solute carrier family 25 member 46).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 3 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:92767 (1 image)
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Charcot-Marie-Tooth disease type 6 | Alliance | Neuropathy, hereditary motor and sensory, type VIB | 616505 |
| pontocerebellar hypoplasia type 1E | Alliance | Pontocerebellar hypoplasia, type 1E | 619303 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mitochondrial carrier domain superfamily | Mitochondrial substrate/solute carrier | Solute carrier family 25 member 46 |
|---|---|---|---|---|
|
UniProtKB:Q6DGU5
|
405 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc25a46-201
(1)
|
Ensembl | 2,053 nt |
Interactions and Pathways
No data available
Plasmids
No data available