Gene
oxr1a
- ID
- ZDB-GENE-080219-14
- Name
- oxidation resistance 1a
- Symbol
- oxr1a Nomenclature History
- Previous Names
-
- oxr1
- oxr2a (1)
- fb25h12
- wu:fb25h12
- zgc:175266
- Type
- protein_coding_gene
- Location
- Chr: 16 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in cerebellar hyplasia/atrophy, epilepsy, and global developmental delay. Is expressed in brain; central nervous system; forebrain; and head. Orthologous to human OXR1 (oxidation resistance 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 8 figures from 4 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 3 figures from Xu et al., 2020
- Cross-Species Comparison
- Alliance
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:A0A8M9PMK0
|
801 | |||
|
UniProtKB:A9JTH8
|
693 | |||
|
UniProtKB:A0A8M9PJL1
|
777 | |||
|
UniProtKB:A0A8M9NZC8
|
775 | |||
|
UniProtKB:A0A8M9PD70
|
804 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available