Gene
slc9a7
- ID
- ZDB-GENE-050913-8
- Name
- solute carrier family 9 member 7
- Symbol
- slc9a7 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to have potassium:proton antiporter activity and sodium:proton antiporter activity. Predicted to be involved in potassium ion transmembrane transport; regulation of intracellular pH; and sodium ion import across plasma membrane. Predicted to localize to plasma membrane and recycling endosome. Human ortholog(s) of this gene implicated in non-syndromic X-linked intellectual disability. Is expressed in female organism; gill; and testis. Orthologous to human SLC9A7 (solute carrier family 9 member A7).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 5 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:7154729 (1 image)
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 |
|---|---|---|---|
| X-linked intellectual developmental disorder 108 | Alliance | Intellectual developmental disorder, X-linked 108 | 301024 |
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 6/7/9 |
|---|---|---|---|---|---|
|
UniProtKB:A9XPA4
|
718 | ||||
|
UniProtKB:F1QI95
|
718 | ||||
|
UniProtKB:A0A8M2BDB4
|
698 | ||||
|
UniProtKB:Q4V9A5
|
718 | ||||
|
UniProtKB:A0A8M3BAH0
|
634 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
slc9a7-202
(1)
|
Havana | 4108 nt |
Interactions and Pathways
No data available
Plasmids
No data available