Gene
slc26a5
- ID
- ZDB-GENE-030131-1566
- Name
- solute carrier family 26 member 5
- Symbol
- slc26a5 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 4 Mapping Details/Browsers
- Description
- Exhibits anion:anion antiporter activity; oxalate transmembrane transporter activity; and secondary active sulfate transmembrane transporter activity. Involved in anion transport and regulation of membrane potential. Localizes to cytoplasm and plasma membrane. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 61. Is expressed in hair cell; inner ear; lagena; utricle; and yolk syncytial layer. Orthologous to human SLC26A5 (solute carrier family 26 member 5).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 8 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:64064 (5 images)
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 nonsyndromic deafness 61 | Alliance | ?Deafness, autosomal recessive 61 | 613865 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | SLC26A/SulP transporter | SLC26A/SulP transporter domain | STAS domain | STAS domain superfamily | Sulphate anion transporter, conserved site |
|---|---|---|---|---|---|---|
|
UniProtKB:Q7T2C4
|
739 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc26a5-201
(1)
|
Ensembl | 3,505 nt | ||
| mRNA |
slc26a5-202
(1)
|
Ensembl | 2,623 nt |
Interactions and Pathways
No data available
Plasmids
No data available