Comparative

Human disease

cystinuria

MONDO:0009067

Mondo defines it as: “Cystinuria is a renal tubular amino acid transport disorder characterized by recurrent formation of kidneys cystine stones.”

4 disease groups in OMIA reach this disease, through OMIA's own Mondo link or its OMIM numbers. The page shows the chain. It does not say whether an animal is a model of this disease.

Animal diseases

By natural-model score for this disease, highest first. The score says how complete and how well supported each chain is, by stated rules. How the score works.

OMIA group Name Found by Species The chain reached Score
256 Cystinuria, type I - A OMIA's OMIM numbers 2 Target evidence 86.6
1879 Cystinuria, type II - A OMIA's OMIM numbers 1 Target evidence 83.6
1880 Cystinuria, type II - B OMIA's OMIM numbers 1 Target evidence 83.5
2023 Cystinuria, type B OMIA's OMIM numbers 1 Target evidence 83.5

Human genes

Each human gene of these disease groups that Open Targets links to this disease.

Human gene Score Evidence
SLC3A1 0.85 760
SLC7A9 0.84 417

Drugs tested for this disease

Each ChEMBL drug that has been tested for this disease, and the human genes above it acts on, if any. Open Targets gives some drugs, such as most enzyme replacement therapies, no target gene.

Drug Acts on Latest stage for this disease
Penicillamine None of these genes Approved
Tiopronin None of these genes Approved
Bucillamine None of these genes Phase 2
Dapagliflozin None of these genes Phase 2
Tolvaptan None of these genes Unknown

The drug data is ChEMBL's, under CC BY-SA 3.0, and came through Open Targets release 26.09.