Cystinuria Gene Set

Dataset CTD 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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D003555
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Genes

2 genes/proteins associated with the disease Cystinuria from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 2.88009
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1 2.88009