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
- Acts upstream of or within regulation of oocyte maturation and regulation of response to oxidative stress. Predicted to be located in mitochondrion. Predicted to be active in nucleus. Is expressed in several structures, including gill; heart; liver; nervous system; and pleuroperitoneal region. Human ortholog(s) of this gene implicated in cerebellar hyplasia/atrophy, epilepsy, and global developmental delay. 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