molybdenum cofactor deficiency Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of molybdenum cofactor(2-), a cofactor for enzymes including sulfite oxidase, xanthine oxidoreductase, and aldehyde oxidase. (Human Phenotype Ontology, HP_0003570)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003570
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Genes

2 genes associated with the molybdenum cofactor deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MOCS1 molybdenum cofactor synthesis 1
MOCS2 molybdenum cofactor synthesis 2