Gene
slc6a17
- ID
- ZDB-GENE-030131-8187
- Name
- solute carrier family 6 member 17
- Symbol
- slc6a17 Nomenclature History
- Previous Names
-
- fj59a05
- si:dkey-71l10.2
- wu:fj59a05
- Type
- protein_coding_gene
- Location
- Chr: 8 Mapping Details/Browsers
- Description
- Predicted to have neurotransmitter:sodium symporter activity. Predicted to be involved in neutral amino acid transport. Predicted to localize to synaptic vesicle. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human SLC6A17 (solute carrier family 6 member 17).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Shankar et al., 2022
- 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 intellectual developmental disorder 48 | Alliance | Intellectual developmental disorder, autosomal recessive 48 | 616269 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Neutral amino acid SLC6 transporter | Sodium:neurotransmitter symporter | Sodium:neurotransmitter symporter superfamily |
|---|---|---|---|---|
|
UniProtKB:X1WEE1
|
730 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
slc6a17-201
(1)
|
Havana | 3847 nt |
Interactions and Pathways
No data available
Plasmids
No data available