abnormal enamel morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the hard outer coating of the exposed portion of the tooth (Mammalian Phenotype Ontology, MP_0002576)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002576
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29 gene mutations causing the abnormal enamel 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
ANTXR1 anthrax toxin receptor 1
CHUK conserved helix-loop-helix ubiquitous kinase
DMP1 dentin matrix acidic phosphoprotein 1
EDA ectodysplasin A
EDARADD EDAR-associated death domain
ENAM enamelin
FAM20A family with sequence similarity 20, member A
FAM20C family with sequence similarity 20, member C
GJA1 gap junction protein, alpha 1, 43kDa
ITGA11 integrin, alpha 11
KLK4 kallikrein-related peptidase 4
LAMA3 laminin, alpha 3
LRP4 low density lipoprotein receptor-related protein 4
MMP20 matrix metallopeptidase 20
MSX2 msh homeobox 2
NFE2L2 nuclear factor, erythroid 2-like 2
PAX9 paired box 9
POSTN periostin, osteoblast specific factor
PTCH1 patched 1
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
RUNX2 runt-related transcription factor 2
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4
SOSTDC1 sclerostin domain containing 1
SP3 Sp3 transcription factor
SP6 Sp6 transcription factor
TGFB1 transforming growth factor, beta 1