Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
64757
Gene name Gene Name - the full gene name approved by the HGNC.
Mitochondrial amidoxime reducing component 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MTARC1
Synonyms (NCBI Gene) Gene synonyms aliases
MARC1, MOSC1
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q41
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003824 Function Catalytic activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IDA
GO:0005739 Component Mitochondrion IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614126 26189 ENSG00000186205
Protein
UniProt ID Q5VT66
Protein name Mitochondrial amidoxime-reducing component 1 (mARC1) (EC 1.7.-.-) (Molybdenum cofactor sulfurase C-terminal domain-containing protein 1) (MOSC domain-containing protein 1) (Moco sulfurase C-terminal domain-containing protein 1)
Protein function Catalyzes the reduction of N-oxygenated molecules, acting as a counterpart of cytochrome P450 and flavin-containing monooxygenases in metabolic cycles (PubMed:19053771, PubMed:21029045, PubMed:30397129). As a component of prodrug-converting syst
PDB 6FW2
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03476 MOSC_N 55 176 MOSC N-terminal beta barrel domain Domain
PF03473 MOSC 202 333 MOSC domain Domain
Sequence
Sequence length 337
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Phase I - Functionalization of compounds
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Cirrhosis Cirrhosis N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Diabetes Mellitus Associate 34258604
Fatty Liver Associate 32282858, 35411667
Fibrosis Associate 32282858, 32720691, 34258604, 36280732, 36555467
Hepatitis Autoimmune Associate 34949757
Hypertriglyceridemia Associate 36233117
Immunologic Deficiency Syndromes Associate 32282858
Liver Cirrhosis Associate 36555467, 40650184
Liver Diseases Associate 32282858, 34258604, 36555467, 37686209, 40650184
Liver Diseases Inhibit 36555467
Liver Failure Associate 34258604, 34949757