cystinuria Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An amino acid metabolic disorder that involves the formation of cystine stones in the kidneys, ureter, and bladder. (Human Disease Ontology, DOID_9266)
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Genes

2 genes involed in the disease cystinuria from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9