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 located in membrane. Predicted to be active in plasma membrane. Human ortholog(s) of this gene implicated in Brown-Vialetto-Van Laere syndrome 2 and riboflavin deficiency. Orthologous to several human genes including 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 | Length | Oligoribonuclease | Solute carrier family 52, riboflavin transporter |
|---|---|---|---|
|
UniProtKB:A0A0R4IZN4
|
885 | ||
|
UniProtKB:Q7SXU6
|
418 |
| 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