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 have thiamine transmembrane transporter activity. Predicted to be involved in thiamine transport and transmembrane transport. Predicted to localize to 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 | Length | MFS transporter superfamily | Reduced folate carrier |
---|---|---|---|
UniProtKB:E7F340
|
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