Gene
slc22a2
- ID
- ZDB-GENE-040426-2167
- Name
- solute carrier family 22 member 2
- Symbol
- slc22a2 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Enables transmembrane transporter activity. Acts upstream of or within determination of heart left/right asymmetry. Located in plasma membrane. Is expressed in several structures, including eye; heart; liver; pleuroperitoneal region; and skeletal muscle. Human ortholog(s) of this gene implicated in acute kidney failure. Orthologous to several human genes including SLC22A2 (solute carrier family 22 member 2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 3 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:64076 (2 images)
Wild Type Expression Summary
- All Phenotype Data
- 2 figures from Shim et al., 2019
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
Type | InterPro ID | Name |
---|---|---|
Conserved_site | IPR005829 | Sugar transporter, conserved site |
Domain | IPR020846 | Major facilitator superfamily domain |
Family | IPR004749 | Organic cation transport protein/SVOP |
Family | IPR005828 | Major facilitator, sugar transporter-like |
Homologous_superfamily | IPR036259 | MFS transporter superfamily |
Domain Details Per Protein
Protein | Length | Major facilitator, sugar transporter-like | Major facilitator superfamily domain | MFS transporter superfamily | Organic cation transport protein/SVOP | Sugar transporter, conserved site |
---|---|---|---|---|---|---|
UniProtKB:Q7T2C0
|
562 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
slc22a2-201
(1)
|
Ensembl | 2,849 nt |
Interactions and Pathways
No data available
Plasmids
No data available