Cystinuria Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An amino acid metabolic disorder that involves the formation of cystine stones in the kidneys, ureter, and bladder. (Human Disease Ontology, DOID_9266)
External Link http://www.omim.org/entry/220100
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Genes

2 genes associated with the Cystinuria phenotype from the curated ClinVar Gene-Phenotype Associations 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