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
- Enables carboxylic acid transmembrane transporter activity; monoatomic ion transmembrane transporter activity; and secondary active sulfate transmembrane transporter activity. Acts upstream of or within several processes, including chloride transport; oxalate transport; and sulfate transport. Located in cytoplasm and plasma membrane. Is expressed in hair cell; inner ear; lagena; utricle; and yolk syncytial layer. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 61. 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