Gene
slc19a2
- ID
- ZDB-GENE-110411-262
- Name
- solute carrier family 19 member 2
- Symbol
- slc19a2 Nomenclature History
- Previous Names
-
- si:ch211-194e2.2
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to be involved in transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. Human ortholog(s) of this gene implicated in diabetes mellitus; megaloblastic anemia; and thiamine-responsive megaloblastic anemia syndrome. Orthologous to human SLC19A2 (solute carrier family 19 member 2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Wu et al., 2020
- 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 |
---|---|---|---|
thiamine-responsive megaloblastic anemia syndrome | Alliance | Thiamine-responsive megaloblastic anemia syndrome | 249270 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Additional Resources | Length | MFS transporter superfamily | Reduced folate carrier |
---|---|---|---|---|
UniProtKB:E7F340 | InterPro | 463 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
slc19a2-201
(1)
|
Ensembl | 1,596 nt | ||
mRNA |
slc19a2-202
(1)
|
Ensembl | 1,093 nt |
Interactions and Pathways
No data available
Plasmids
No data available