Gene
slc52a2
- ID
- ZDB-GENE-030131-2552
- Name
- solute carrier family 52 member 2
- Symbol
- slc52a2 Nomenclature History
- Previous Names
-
- fc11c06
- gpr172a
- wu:fc11c06
- zgc:63774
- Type
- protein_coding_gene
- Location
- Chr: 19 Mapping Details/Browsers
- Description
- Predicted to enable riboflavin transmembrane transporter activity. Predicted to be involved in riboflavin transport. Predicted to be active in plasma membrane. Human ortholog(s) of this gene implicated in Brown-Vialetto-Van Laere syndrome 2. Orthologous to human SLC52A2 (solute carrier family 52 member 2).
- 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:63774 (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 |
|---|---|---|---|
| Brown-Vialetto-Van Laere syndrome 2 | Alliance | Brown-Vialetto-Van Laere syndrome 2 | 614707 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Additional Resources | Length | Oligoribonuclease | Solute carrier family 52, riboflavin transporter |
|---|---|---|---|---|
| UniProtKB:A0A0R4IZN4 | InterPro | 885 | ||
| UniProtKB:Q7SXU6 | InterPro | 418 | ||
| UniProtKB:A0A8M1PEB3 | InterPro | 438 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc52a2-201
(1)
|
Ensembl | 1,803 nt |
Interactions and Pathways
No data available
Plasmids
No data available