kidney medulla atrophy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description acquired diminution of the size of the inner portion of the kidney consisting of the renal pyramids, associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal changes (Mammalian Phenotype Ontology, MP_0011422)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011422
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Genes

9 gene mutations causing the kidney medulla atrophy 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)
APRT adenine phosphoribosyltransferase
AQP2 aquaporin 2 (collecting duct)
GLIS2 GLIS family zinc finger 2
REN renin
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
VAMP8 vesicle-associated membrane protein 8