abnormal enamel rod pattern Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the orientation of the structural unit of tooth enamel (Mammalian Phenotype Ontology, MP_0002649)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002649
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4 gene mutations causing the abnormal enamel rod pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AMELY amelogenin, Y-linked
FAM20A family with sequence similarity 20, member A
MMP20 matrix metallopeptidase 20
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)