Molybdenum cofactor deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:C535811
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Genes

3 genes/proteins associated with the disease Molybdenum cofactor deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MOCS2 molybdenum cofactor synthesis 2 2.88009
MOCS1 molybdenum cofactor synthesis 1 2.88009
GPHN gephyrin 2.88009