urea cycle disorder Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An amino acid metabolic disorder that involves a deficiency of one of the enzymes in the urea cycle which is responsible for removing ammonia from the blood stream. (Human Disease Ontology, DOID_9267)
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Genes

4 genes involed in the disease urea cycle disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ARG1 arginase 1
ASS1 argininosuccinate synthase 1
OTC ornithine carbamoyltransferase
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13