fused kidneys Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a defect in which there is a single malformed organ resulting from partial or complete fusion of the two renal anlage (Mammalian Phenotype Ontology, MP_0003605)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003605
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Genes

4 gene mutations causing the fused kidneys phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
DACT1 dishevelled-binding antagonist of beta-catenin 1
FOXD1 forkhead box D1
SPRY1 sprouty homolog 1, antagonist of FGF signaling (Drosophila)