Gene
slc46a1
- ID
- ZDB-GENE-040426-1012
- Name
- solute carrier family 46 member 1
- Symbol
- slc46a1 Nomenclature History
- Previous Names
-
- zgc:56400 (1)
- Type
- protein_coding_gene
- Location
- Chr: 15 Mapping Details/Browsers
- Description
- Predicted to have folic acid binding activity. Predicted to be involved in transmembrane transport. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in hereditary folate malabsorption. Orthologous to human SLC46A1 (solute carrier family 46 member 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:56400 (1 image)
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 |
|---|---|---|---|
| hereditary folate malabsorption | Alliance | Folate malabsorption, hereditary | 229050 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Major facilitator superfamily | MFS transporter superfamily |
|---|---|---|---|
|
UniProtKB:Q7ZWG6
|
481 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc46a1-201
(1)
|
Ensembl | 1,940 nt |
Interactions and Pathways
No data available
Plasmids
No data available