Msrb3 - methionine sulfoxide reductase B3 Gene

Also Known as MsrB2; I-8-23; D430026P16Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 320183

Summary

Predicted to enable peptide-methionine (R)-S-oxide reductase activity and zinc ion binding activity. Predicted to be involved in protein repair. Predicted to be located in endoplasmic reticulum and mitochondrion. Predicted to be active in cytoplasm. Is expressed in several structures, including heart; inner ear; jaw; limb; and skeleton. Used to study autosomal recessive nonsyndromic deafness 74. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 74. Orthologous to human MSRB3 (methionine sulfoxide reductase B3). [provided by Alliance of Genome Resources, Apr 2022]

Msrb3 Products (3)

mRNA Protein Name
NM_001406399.1 NP_001393328.1 methionine-R-sulfoxide reductase B3, mitochondrial isoform 2
NM_001406400.1 NP_001393329.1 methionine-R-sulfoxide reductase B3, mitochondrial isoform 3
NM_177092.5 NP_796066.1 methionine-R-sulfoxide reductase B3, mitochondrial isoform 1

Gene Ontology

  • Cellular Component
Cellular Component GO Annotation Evidence References Source
NOT located in mitochondrion IDA
IDA: Inferred from direct assay
15249228 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

methionine-R-sulfoxide reductase B3, mitochondrial

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (3)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS08728 MSRB3 Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS19718 Msrb3 Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS26214 Msrb3 Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Msrb3 NCBI NCBI:253827