cystinuria Gene Set

Dataset GAD Gene-Disease Associations
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

3 genes associated with the disease cystinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9