ameloblast degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a retrogressive impairment of function or destruction of the epithelial cells of the inner later of the enamel organ of the developing tooth (Mammalian Phenotype Ontology, MP_0000129)
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4 gene mutations causing the ameloblast degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
MSX2 msh homeobox 2
NFE2L2 nuclear factor, erythroid 2-like 2
TGFB1 transforming growth factor, beta 1