abnormality of primary teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the primary tooth. (Human Phenotype Ontology, HP_0006481)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006481
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Genes

33 genes associated with the abnormality of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
ALPL alkaline phosphatase, liver/bone/kidney
BCOR BCL6 corepressor
CLCN7 chloride channel, voltage-sensitive 7
COL3A1 collagen, type III, alpha 1
CTSC cathepsin C
CTSK cathepsin K
EDAR ectodysplasin A receptor
EDARADD EDAR-associated death domain
EHMT1 euchromatic histone-lysine N-methyltransferase 1
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
FERMT1 fermitin family member 1
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FIG4 FIG4 phosphoinositide 5-phosphatase
FLNA filamin A, alpha
GJA1 gap junction protein, alpha 1, 43kDa
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
MSX1 msh homeobox 1
PTH1R parathyroid hormone 1 receptor
RAB23 RAB23, member RAS oncogene family
RUNX2 runt-related transcription factor 2
SNX10 sorting nexin 10
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TMCO1 transmembrane and coiled-coil domains 1
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
TRAF6 TNF receptor-associated factor 6, E3 ubiquitin protein ligase
UBR1 ubiquitin protein ligase E3 component n-recognin 1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
WNT10A wingless-type MMTV integration site family, member 10A