pelvic kidney Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect in which a kidney is located in an abnormal anatomic position within the pelvis. (Human Phenotype Ontology, HP_0000125)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011361
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Genes

3 gene mutations causing the pelvic kidney phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
FOXD1 forkhead box D1
NOG noggin