Gene
slc25a22b
- ID
- ZDB-GENE-110408-66
- Name
- solute carrier family 25 member 22b
- Symbol
- slc25a22b Nomenclature History
- Previous Names
-
- si:ch73-219d10.1
- Type
- protein_coding_gene
- Location
- Chr: 7 Mapping Details/Browsers
- Description
- Predicted to have L-aspartate transmembrane transporter activity and L-glutamate transmembrane transporter activity. Predicted to be involved in L-glutamate transmembrane transport; aspartate transmembrane transport; and malate-aspartate shuttle. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in early infantile epileptic encephalopathy 3. Orthologous to human SLC25A22 (solute carrier family 25 member 22).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| developmental and epileptic encephalopathy 3 | Alliance | Developmental and epileptic encephalopathy 3 | 609304 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mitochondrial carrier domain superfamily | Mitochondrial carrier protein | Mitochondrial Solute Carrier | Mitochondrial substrate/solute carrier |
|---|---|---|---|---|---|
|
UniProtKB:F8W3S7
|
318 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc25a22b-201
(1)
|
Ensembl | 1,545 nt | ||
| mRNA |
slc25a22b-202
(1)
|
Ensembl | 1,431 nt |
Interactions and Pathways
No data available
Plasmids
No data available