absent metanephros Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the primordium of the permanent kidney, which develops later than and caudal to the mesonephros, from the mesonephric duct and nephrogenic cord (Mammalian Phenotype Ontology, MP_0011366)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011366
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Genes

8 gene mutations causing the absent metanephros phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFRL1 fibroblast growth factor receptor-like 1
GREM1 gremlin 1, DAN family BMP antagonist
LAMC1 laminin, gamma 1 (formerly LAMB2)
LHX1 LIM homeobox 1
OSR1 odd-skipped related transciption factor 1
PAX2 paired box 2
SIX1 SIX homeobox 1
WT1 Wilms tumor 1