abnormal ameloblast morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the epithelial cells of the inner layer of the enamel organ of the developing tooth (Mammalian Phenotype Ontology, MP_0002650)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002650
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15 gene mutations causing the abnormal ameloblast morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AMBN ameloblastin (enamel matrix protein)
AMELY amelogenin, Y-linked
BCL11B B-cell CLL/lymphoma 11B (zinc finger protein)
FAM20A family with sequence similarity 20, member A
LAMA3 laminin, alpha 3
MMP20 matrix metallopeptidase 20
MSX2 msh homeobox 2
NFE2L2 nuclear factor, erythroid 2-like 2
PAX9 paired box 9
POSTN periostin, osteoblast specific factor
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
SP3 Sp3 transcription factor
SP6 Sp6 transcription factor
TGFB1 transforming growth factor, beta 1