Gene
slc12a2l
- ID
- ZDB-GENE-210112-1
- Name
- solute carrier family 12 member 2-like
- Symbol
- slc12a2l Nomenclature History
- Previous Names
-
- slc12a2b (1)
- Type
- protein_coding_gene
- Location
- Chr: 8 Mapping Details/Browsers
- Description
- Predicted to enable ammonium channel activity and sodium:potassium:chloride symporter activity. Acts upstream of or within myelination. Predicted to be located in plasma membrane. Predicted to be active in apical plasma membrane. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 78 and middle cerebral artery infarction. Orthologous to human SLC12A2 (solute carrier family 12 member 2).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Domain | IPR004841 | Amino acid permease/ SLC12A domain |
| Domain | IPR013612 | Amino acid permease, N-terminal |
| Domain | IPR018491 | SLC12A transporter, C-terminal |
| Family | IPR002443 | Solute carrier family 12 member 1/2 |
| Family | IPR002444 | Solute carrier family 12 member 2 |
| Family | IPR004842 | SLC12A transporter family |
Domain Details Per Protein
| Protein | Additional Resources | Length | Amino acid permease, N-terminal | Amino acid permease/ SLC12A domain | SLC12A transporter, C-terminal | SLC12A transporter family | Solute carrier family 12 member 1/2 | Solute carrier family 12 member 2 |
|---|---|---|---|---|---|---|---|---|
| UniProtKB:A0A8M1RPE8 | InterPro | 1091 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available