1. Gene
  2. Msrb3 - methionine sulfoxide reductase B3 Gene

Msrb3 - methionine sulfoxide reductase B3 Gene

种属: Mus musculus

同用名: MsrB2; I-8-23; D430026P16Rik

基因 ID: 320183 | 基因类型: protein coding

关于 Msrb3

功能概要

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 基因产物(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
基因本体论
  • 细胞组分
细胞组分 GO 注释 逻辑证据 参考文献 来源
NOT located in mitochondrion IDA
IDA: 通过直接分析推断
15249228 MGI
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断
蛋白主名 其他名称

methionine-R-sulfoxide reductase B3, mitochondrial

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Msrb3 NCBI NCBI:253827