abnormal molar crown morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the part of a molar that is covered by enamel (Mammalian Phenotype Ontology, MP_0003932)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003932
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16 gene mutations causing the abnormal molar crown morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AMBN ameloblastin (enamel matrix protein)
AMELY amelogenin, Y-linked
CHUK conserved helix-loop-helix ubiquitous kinase
DLX5 distal-less homeobox 5
EDA ectodysplasin A
EDARADD EDAR-associated death domain
LRP4 low density lipoprotein receptor-related protein 4
LRP6 low density lipoprotein receptor-related protein 6
NGFR nerve growth factor receptor
NKX2-3 NK2 homeobox 3
OSTM1 osteopetrosis associated transmembrane protein 1
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SOSTDC1 sclerostin domain containing 1
SP6 Sp6 transcription factor
SPRY2 sprouty homolog 2 (Drosophila)