Gene

msrb3

ID
ZDB-GENE-040625-74
Name
methionine sulfoxide reductase B3
Symbol
msrb3 Nomenclature History
Previous Names
  • wu:fc07g04
  • zgc:86909
Type
protein_coding_gene
Location
Chr: 4 Mapping Details/Browsers
Description
Predicted to have peptide-methionine (R)-S-oxide reductase activity. Involved in inner ear development. Predicted to localize to cytoplasm. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 74. Is expressed in heart rudiment; heart tube; inner ear; and myotome. Orthologous to human MSRB3 (methionine sulfoxide reductase B3).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
10 figures from 3 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
5 figures from Shen et al., 2015
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With msrb3 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive nonsyndromic deafness 74 Alliance Deafness, autosomal recessive 74 613718
Associated With msrb3 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR002579 Peptide methionine sulphoxide reductase MrsB domain
Family IPR028427 Peptide methionine sulfoxide reductase MsrB
Homologous_superfamily IPR011057 Mss4-like superfamily
Domain Details Per Protein
Protein Length Mss4-like superfamily Peptide methionine sulfoxide reductase MsrB Peptide methionine sulphoxide reductase MrsB domain
UniProtKB:A0A8M1P8M4 200
UniProtKB:Q5TZH8 187
UniProtKB:Q5TZH6 186
Transcripts
Genome Browsers
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