abnormal keratinocyte migration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the movement of keratinocyes or their precursors to the appropriate location in the body (Mammalian Phenotype Ontology, MP_0012192)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012192
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5 gene mutations causing the abnormal keratinocyte migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLIC4 chloride intracellular channel 4
DACT2 dishevelled-binding antagonist of beta-catenin 2
EPPK1 epiplakin 1
ILK integrin-linked kinase
PPM1A protein phosphatase, Mg2+/Mn2+ dependent, 1A