abnormal nephrogenic mesenchyme morphogenesis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the embryonic connective tissue made up of loosely aggregated mesenchymal cells, supported by interlaminar jelly, that gives rise to the developing nephron (Mammalian Phenotype Ontology, MP_0010987)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010987
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Genes

5 gene mutations causing the abnormal nephrogenic mesenchyme morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFRL1 fibroblast growth factor receptor-like 1
FOXD1 forkhead box D1
OSR1 odd-skipped related transciption factor 1
PBX1 pre-B-cell leukemia homeobox 1
WNT4 wingless-type MMTV integration site family, member 4