kidney papillary atrophy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description acquired diminution of the size of the apex (tip) of a renal pyramid 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_0011304)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011304
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Genes

8 gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AQP2 aquaporin 2 (collecting duct)
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
FSTL1 follistatin-like 1
NFAT5 nuclear factor of activated T-cells 5, tonicity-responsive
REN renin
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1