Gene
otog
- ID
- ZDB-GENE-120228-1
- Name
- otogelin
- Symbol
- otog Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 7 Mapping Details/Browsers
- Description
- Predicted to enable alpha-L-arabinofuranosidase activity and structural molecule activity. Acts upstream of or within otolith formation; otolith tethering; and proprioception. Predicted to be located in extracellular region. Is expressed in otic vesicle and vestibuloauditory system. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 18B. Orthologous to human OTOG (otogelin).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 6 figures from 4 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 26 figures from 6 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| autosomal recessive nonsyndromic deafness 18B | Alliance | Deafness, autosomal recessive 18B | 614945 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance