abnormal kidney inner medulla morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the inner medullary region of the adult kidney containing collecting ducts and the long loops of Henle (Mammalian Phenotype Ontology, MP_0011333)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011333
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7 gene mutations causing the abnormal kidney inner medulla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
FGF10 fibroblast growth factor 10
FGF7 fibroblast growth factor 7
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
SDC4 syndecan 4