Cystinuria Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
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 Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 4.0
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1 4.0