MOCS1 Products

Description

Molybdenum cofactor biosynthesis is a conserved pathway leading to the biological activation of molybdenum. The protein encoded by this gene is involved in molybdenum cofactor biosynthesis. This gene was originally thought to produce a bicistronic mRNA with the potential to produce two proteins (MOCS1A and MOCS1B) from adjacent open reading frames. However, only the first open reading frame (MOCS1A) has been found to encode a protein from the putative bicistronic mRNA. Two of the splice variants found for this gene express proteins (MOCS1A-MOCS1B) that result from a fusion between the two open reading frames. This gene is defective in patients with molybdenum cofactor deficiency, type A. (provided by RefSeq)

Bioinformatics

Entrez	4337 Human
Product By Gene ID	4337
Alternate Names	molybdenum cofactor synthesis 1

Diseases related to MOCS1

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Combined Molybdoflavoprotein Enzyme Deficiency
Sulfocysteinuria
Inborn Errors Of Metabolism
Trauma, Nervous System
Convulsion Neonatal
Metabolic Diseases
Brain Ischemia
Encephalomalacia
Brain Injuries
Microcephaly
Hereditary Diseases
Developmental Delay (disorder)
Nervous System Disorder
Encephalopathies
Mutation, Out-of-frame
Melanoma
Congenital Musculoskeletal Anomalies
Hypoxia

Pathways for MOCS1

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Translation
Localization
Mrna Splicing
Cell Death
Translation Reinitiation
Bone Development
Pathogenesis

PTMs for MOCS1

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Cleavage

Bioinformatics Tool for MOCS1

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