absent kidney papilla Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the apex (tip) of a renal pyramid i.e. the location where each medullary pyramid empties urine into a minor calyx (Mammalian Phenotype Ontology, MP_0011303)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011303
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2 gene mutations causing the absent kidney papilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
ESRRG estrogen-related receptor gamma