Gene
slc9a1b
- ID
- ZDB-GENE-080225-42
- Name
- solute carrier family 9 member A1b
- Symbol
- slc9a1b Nomenclature History
- Previous Names
-
- nhe1 (1)
- slc9a1
- Type
- protein_coding_gene
- Location
- Chr: 17 Mapping Details/Browsers
- Description
- Predicted to have sodium:proton antiporter activity. Predicted to be involved in regulation of pH; sodium ion transport; and transmembrane transport. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in autosomal recessive spinocerebellar ataxia 19 and congestive heart failure. Is expressed in blood and gill. Orthologous to human SLC9A1 (solute carrier family 9 member A1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from Yan et al., 2007
- 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:A0A8M9PKX4
|
382 | |||||
|
UniProtKB:A0A8M9PNY2
|
494 | |||||
|
UniProtKB:A9XP99
|
653 | |||||
|
UniProtKB:A0A8M9PEE6
|
598 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
slc9a1b-202
(1)
|
Havana | 390 nt |
Interactions and Pathways
No data available
Plasmids
No data available