kidney papillary hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, of the apex of the renal pyramid that normally projects into a calyx (Mammalian Phenotype Ontology, MP_0011565)
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5 gene mutations causing the kidney papillary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
FGF7 fibroblast growth factor 7
REN renin