abnormal kidney pyramid morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the conical mass of tissue, containing part of the secreting and collecting tubules, whose base faces the renal cortex (Mammalian Phenotype Ontology, MP_0004192)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004192
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Genes

18 gene mutations causing the abnormal kidney pyramid morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AQP2 aquaporin 2 (collecting duct)
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
ESRRG estrogen-related receptor gamma
FGF7 fibroblast growth factor 7
FSTL1 follistatin-like 1
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
LEPR leptin receptor
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MMP17 matrix metallopeptidase 17 (membrane-inserted)
NFAT5 nuclear factor of activated T-cells 5, tonicity-responsive
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
REN renin
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
UMOD uromodulin