MSRB2 - methionine sulfoxide reductase B2 Gene

Also Known as CBS1; MSRB; PILB; CBS-1; CGI-131

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 22921

About MSRB2

Cytogenetic location: 10p12.2 Genomic coordinates (GRCh38): 10:23,095,579-23,122,013 (from NCBI)

This gene has 3 transcripts (splice variants), 101 orthologues and 3 paralogues. Ubiquitous expression in heart (RPKM 17.2), liver (RPKM 8.9) and 24 other tissues.

Summary

Predicted to enable actin binding activity; peptide-methionine (R)-S-oxide reductase activity; and zinc ion binding activity. Predicted to be involved in actin filament polymerization and protein repair. Predicted to be located in mitochondrion. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

MSRB2 Products (1)

mRNA Protein Name
NM_012228.4 NP_036360.3 methionine-R-sulfoxide reductase B2, mitochondrial precursor
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
27499296 GOA
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

MSRB2 Protein Structure

SelR

SelR: SelR domain (52 - 179)

  • 0
  • 100
  • 182 a.a.
Protein Preferred Names Protein Names

methionine-R-sulfoxide reductase B2, mitochondrial

  • pilin-like transcription factor

MSRB2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
MSRB2 Q9Y3D2 JPH3 Homo sapiens Q8WXH2 32814053
Intra
MSRB2 Q9Y3D2 JPH3 Homo sapiens Q8WXH2 32814053
Intra
MSRB2 Q9Y3D2 JPH3 Homo sapiens Q8WXH2 32814053
Intra
MSRB2 Q9Y3D2 APOE Homo sapiens P02649 32814053
Intra
MSRB2 Q9Y3D2 APOE Homo sapiens P02649 32814053
Intra
MSRB2 Q9Y3D2 APOE Homo sapiens P02649 32814053
Intra
MSRB2 Q9Y3D2 APBB2 Homo sapiens Q92870-2 32814053
Intra
MSRB2 Q9Y3D2 APBB2 Homo sapiens Q92870-2 32814053
Intra
MSRB2 Q9Y3D2 APBB2 Homo sapiens Q92870-2 32814053
Intra
MSRB2 Q9Y3D2 TRAF2 Homo sapiens Q12933 32296183
Intra
MSRB2 Q9Y3D2 TRAF2 Homo sapiens Q12933 32296183
Intra
MSRB2 Q9Y3D2 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
MSRB2 Q9Y3D2 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
MSRB2 Q9Y3D2 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
MSRB2 Q9Y3D2 NDUFV2 Homo sapiens P19404 32814053
Intra
MSRB2 Q9Y3D2 NDUFV2 Homo sapiens P19404 32814053
Intra
MSRB2 Q9Y3D2 NDUFV2 Homo sapiens P19404 32814053
Intra
MSRB2 Q9Y3D2 NDRG1 Homo sapiens Q92597 32814053
Intra
MSRB2 Q9Y3D2 NDRG1 Homo sapiens Q92597 32814053
Intra
MSRB2 Q9Y3D2 NDRG1 Homo sapiens Q92597 32814053
Intra
MSRB2 Q9Y3D2 GFAP Homo sapiens P14136 32814053
Intra
MSRB2 Q9Y3D2 GFAP Homo sapiens P14136 32814053
Intra
MSRB2 Q9Y3D2 GFAP Homo sapiens P14136 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hypomagnesemia 6, Renal
  • Renal Hypomagnesemia 6

  • HOMG6

  • Renal Hypomagnesemia-6

  • Hypomagnesemia 6

  • Hypomagnesemia, Type 6, Renal

Neu-Laxova Syndrome 2
  • NLS2

Myotonia Congenita
  • Congenital Myotonia, Autosomal Dominant Form

  • Congenital Myotonia

  • Thomsen And Becker Disease

  • Thomsen Disease

  • Thomsen'S Disease

  • Generalized Myotonia Of Thomsen

  • Congenital Myotonic Muscular Dystrophy

  • Myotonia Congenita Nos

Atrial Septal Defect 1
  • ASD1

  • Atrial Heart Septal Defect 1

  • Asd

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta MSRB2 VGNC VGNC:74786
Bos taurus MSRB2 VGNC VGNC:31706
Rattus norvegicus MSRB2 RGD RGD:1306026
Mus musculus MSRB2 MGD MGI:1923717
Canis familiaris MSRB2 VGNC VGNC:43450
Others MSRB2 NCBI