Gene Gene information from NCBI Gene database.
Entrez ID 51734
Gene name Methionine sulfoxide reductase B1
Gene symbol MSRB1
Synonyms (NCBI Gene)
HSPC270SELENORSELENOXSELRSELXSEPX1SepR
Chromosome 16
Chromosome location 16p13.3
Summary The protein encoded by this gene belongs to the methionine-R-sulfoxide reductase B (MsrB) family. Members of this family function as repair enzymes that protect proteins from oxidative stress by catalyzing the reduction of methionine-R-sulfoxides to methi
miRNA miRNA information provided by mirtarbase database.
27
miRTarBase ID miRNA Experiments Reference
MIRT045669 hsa-miR-149-5p CLASH 23622248
MIRT656122 hsa-miR-3145-5p HITS-CLIP 23824327
MIRT656120 hsa-miR-6793-3p HITS-CLIP 23824327
MIRT656121 hsa-miR-937-5p HITS-CLIP 23824327
MIRT656119 hsa-miR-627-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
28
GO ID Ontology Definition Evidence Reference
GO:0002376 Process Immune system process IEA
GO:0003779 Function Actin binding IEA
GO:0003779 Function Actin binding ISS
GO:0005515 Function Protein binding IPI 23805218, 28579431, 32296183
GO:0005634 Component Nucleus IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606216 14133 ENSG00000198736
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NZV6
Protein name Methionine-R-sulfoxide reductase B1 (MsrB1) (EC 1.8.4.12) (EC 1.8.4.14) (Selenoprotein X) (SelX)
Protein function Methionine-sulfoxide reductase that specifically reduces methionine (R)-sulfoxide back to methionine. While in many cases, methionine oxidation is the result of random oxidation following oxidative stress, methionine oxidation is also a post-tra
PDB 3MAO
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01641 SelR 5 105 SelR domain Family
Sequence
Sequence length 116
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Protein repair
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
PSYCHIATRIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 23805218, 36497178
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 17519015
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 34719306
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 25541970, 34719306
★☆☆☆☆
Found in Text Mining only
Dermatitis Atopic Associate 36497178
★☆☆☆☆
Found in Text Mining only
Osteoarthritis Associate 37033956
★☆☆☆☆
Found in Text Mining only
Osteosarcoma Associate 34719306
★☆☆☆☆
Found in Text Mining only
Rectal Neoplasms Associate 25541970
★☆☆☆☆
Found in Text Mining only
Respiratory Distress Syndrome Associate 37336980
★☆☆☆☆
Found in Text Mining only
Sepsis Associate 37336980
★☆☆☆☆
Found in Text Mining only