abnormal kidney medulla development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the differentiation of the inner portion of the kidney consisting of the renal pyramids (Mammalian Phenotype Ontology, MP_0003613)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003613
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2 gene mutations causing the abnormal kidney medulla development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
RET ret proto-oncogene