Gene
slc17a9a
- ID
- ZDB-GENE-081021-1
- Name
- solute carrier family 17 member 9a
- Symbol
- slc17a9a Nomenclature History
- Previous Names
-
- gb:dr724030 (1)
- si:ch211-196c10.7
- Type
- protein_coding_gene
- Location
- Chr: 8 Mapping Details/Browsers
- Description
- Predicted to have transmembrane transporter activity. Predicted to be involved in anion transport. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in porokeratosis. Orthologous to human SLC17A9 (solute carrier family 17 member 9).
- 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
- 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 |
---|---|---|---|
Porokeratosis 8, disseminated superficial actinic type | 616063 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Major facilitator superfamily | Major facilitator superfamily domain | MFS transporter superfamily | Solute carrier family 17 member 9-like | Sugar transporter, conserved site |
---|---|---|---|---|---|---|
UniProtKB:E9QCB4
|
458 |
Type | Name | Length (nt) | Analysis |
---|---|---|---|
mRNA |
slc17a9a-201
(1)
|
1843 nt |
Interactions and Pathways
No data available
Plasmids
No data available