Gene
slc9a1a
- ID
- ZDB-GENE-170609-1
- Name
- solute carrier family 9 member A1a
- Symbol
- slc9a1a Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 16 Mapping Details/Browsers
- Description
- Predicted to enable sodium:proton antiporter activity. Predicted to act upstream of or within proton transmembrane transport; regulation of pH; and sodium ion transport. Predicted to be located in basolateral plasma membrane and lateral plasma membrane. Human ortholog(s) of this gene implicated in autosomal recessive spinocerebellar ataxia 19 and congestive heart failure. Orthologous to human SLC9A1 (solute carrier family 9 member A1).
- Genome Resources
-
- Alliance (1)
- Gene:101885761 (1)
- 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
- 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 |
|---|---|---|---|
| autosomal recessive spinocerebellar ataxia 19 | Alliance | Lichtenstein-Knorr syndrome | 616291 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Additional Resources | Length | Cation/H+ exchanger, CPA1 family | Cation/H+ exchanger, transmembrane domain | Na+/H+ exchanger | Sodium/hydrogen exchanger 1-like | Sodium/hydrogen exchanger, regulatory region |
|---|---|---|---|---|---|---|---|
| UniProtKB:A0A8M2BKS9 | InterPro | 766 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance