dilated kidney collecting duct Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description stretched or widened aperture of the luminal space of the collecting ducts (Mammalian Phenotype Ontology, MP_0004860)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004860
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18 gene mutations causing the dilated kidney collecting duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
AQP2 aquaporin 2 (collecting duct)
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
DCHS1 dachsous cadherin-related 1
DLG1 discs, large homolog 1 (Drosophila)
DLG5 discs, large homolog 5 (Drosophila)
EGFR epidermal growth factor receptor
FOXD1 forkhead box D1
INVS inversin
MKS1 Meckel syndrome, type 1
NEK8 NIMA-related kinase 8
NPHP3 nephronophthisis 3 (adolescent)
PCCA propionyl CoA carboxylase, alpha polypeptide
SCTR secretin receptor
UMOD uromodulin
UOX urate oxidase, pseudogene
VAMP8 vesicle-associated membrane protein 8