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MSRA (methionine sulfoxide reductase A)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4482
Gene nameGene Name - the full gene name approved by the HGNC.
Methionine sulfoxide reductase A
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
MSRA
SynonymsGene synonyms aliases
PMSR
ChromosomeChromosome number
8
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8p23.1
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a ubiquitous and highly conserved protein that carries out the enzymatic reduction of methionine sulfoxide to methionine. Human and animal studies have shown the highest levels of expression in kidney and nervous tissue. The protein func
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022647 hsa-miR-124-3p Microarray 18668037
MIRT1161808 hsa-miR-1228 CLIP-seq
MIRT1161809 hsa-miR-198 CLIP-seq
MIRT1161810 hsa-miR-338-3p CLIP-seq
MIRT1161811 hsa-miR-342-3p CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005654 Component Nucleoplasm IDA
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005739 Component Mitochondrion IEA
GO:0005829 Component Cytosol IDA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q9UJ68
Protein name Mitochondrial peptide methionine sulfoxide reductase (EC 1.8.4.11) (Peptide-methionine (S)-S-oxide reductase) (Peptide Met(O) reductase) (Protein-methionine-S-oxide reductase) (PMSR)
Protein function Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01625 PMSR
67 221
Peptide methionine sulfoxide reductase
Family
Sequence
Sequence length 235
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
Reactome
    Protein repair
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Asthma Chronic obstructive asthma (with obstructive pulmonary disease) rs324981, rs121912630, rs150116809, rs4950928, rs708494, rs1581842283 30657218
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 21679298, 28991256, 18506707, 26198764, 30285260, 31374203
Unknown
Disease name Disease term dbSNP ID References
Anxiety disorder Anxiety 29942085
Barrett esophagus Barrett Esophagus rs41341748 27527254
Esophageal cancer Adenocarcinoma Of Esophagus 27527254
Mental depression Unipolar Depression, Major Depressive Disorder rs587778876, rs587778877 29559929

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