absent enamel Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the hard outer coating of the exposed portion of the tooth (Mammalian Phenotype Ontology, MP_0003404)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003404
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7 gene mutations causing the absent enamel phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AMBN ameloblastin (enamel matrix protein)
ENAM enamelin
FAM20A family with sequence similarity 20, member A
FAM20C family with sequence similarity 20, member C
PAX9 paired box 9
SP3 Sp3 transcription factor
SP6 Sp6 transcription factor