Gene
slitrk6
- ID
- ZDB-GENE-030131-2816
- Name
- SLIT and NTRK-like family, member 6
- Symbol
- slitrk6 Nomenclature History
- Previous Names
-
- wu:fc18f06
- Type
- protein_coding_gene
- Location
- Chr: 1 Mapping Details/Browsers
- Description
- Predicted to be involved in axonogenesis. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in high myopia-sensorineural deafness syndrome. Is expressed in nervous system and otic vesicle. Orthologous to human SLITRK6 (SLIT and NTRK like family member 6).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 7 figures from Round et al., 2014
- 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 |
|---|---|---|---|
| high myopia-sensorineural deafness syndrome | Alliance | Deafness and myopia | 221200 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Cysteine-rich flanking region, C-terminal | Leucine-rich repeat | Leucine-rich repeat domain superfamily | Leucine-rich repeat, typical subtype |
|---|---|---|---|---|---|
|
UniProtKB:A0A0R4IS19
|
830 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available