kidney medulla cysts Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal membranous sacs appearing in the inner portion of the kidney which consists of the renal pyramids (Mammalian Phenotype Ontology, MP_0011307)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011307
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Genes

10 gene mutations causing the kidney medulla cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
AQP2 aquaporin 2 (collecting duct)
BCL2 B-cell CLL/lymphoma 2
GPC3 glypican 3
INVS inversin
NEK8 NIMA-related kinase 8
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
PAX2 paired box 2
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD2 polycystic kidney disease 2 (autosomal dominant)