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
- 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 | Length | Cation/H+ exchanger | Cation/H+ exchanger, CPA1 family | Na+/H+ exchanger | Sodium/hydrogen exchanger 1-like | Sodium/hydrogen exchanger, regulatory region |
|---|---|---|---|---|---|---|
|
UniProtKB:A0A8M2BKS9
|
766 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance