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
Expression
All Expression Data
8 figures from 4 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
3 figures from Xu et al., 2020
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With oxr1a Human Ortholog
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
Associated With oxr1a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR006571 TLDc domain
Domain IPR018392 LysM domain
Homologous_superfamily IPR036779 LysM domain superfamily
Domain Details Per Protein
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations