Gene
oxr1b
- ID
- ZDB-GENE-030131-2438
- Name
- oxidation resistance 1b
- Symbol
- oxr1b Nomenclature History
- Previous Names
-
- fc07g10
- si:dkeyp-84f11.5
- wu:fc07g10
- Type
- protein_coding_gene
- Location
- Chr: 19 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in cerebellar hyplasia/atrophy, epilepsy, and global developmental delay. Is expressed in central nervous system; head; lateral line ganglion; and olfactory pit. Orthologous to human OXR1 (oxidation resistance 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 10 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| cerebellar hyplasia/atrophy, epilepsy, and global developmental delay | Alliance | Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay | 213000 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | LysM domain | LysM domain superfamily | TLDc domain |
|---|---|---|---|---|
|
UniProtKB:F1Q4W8
|
749 | |||
|
UniProtKB:A0A8M3AK20
|
240 | |||
|
UniProtKB:I3ISS4
|
841 | |||
|
UniProtKB:A0A8M2B610
|
814 |
Interactions and Pathways
No data available
Plasmids
No data available