Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1747
Gene Symbol: DLX3
DLX3 		0.140 GeneticVariation disease BEFREE Previously, the DLX3 c.561_562delCT mutation was associated with autosomal dominant amelogenesis imperfecta with taurodontism. 18203197 2008
Entrez Id: 1747
Gene Symbol: DLX3
DLX3 		0.140 GeneticVariation disease BEFREE Recently, another DLX3 gene mutation (c.561_562delCT) was reported to cause amelogenesis imperfecta with taurodontism (AIHHT). 18362318 2008
Entrez Id: 1747
Gene Symbol: DLX3
DLX3 		0.140 Biomarker disease BEFREE Late genes expressed during root formation (ALPL and DLX3) are associated with cementum agenesis (hypophosphatasia) and taurodontism. 17552940 2007
Entrez Id: 1747
Gene Symbol: DLX3
DLX3 		0.140 GeneticVariation disease BEFREE DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism. 15666299 2005
Entrez Id: 1747
Gene Symbol: DLX3
DLX3 		0.140 Biomarker disease HPO
Entrez Id: 1747
Gene Symbol: DLX3
DLX3 		0.140 CausalMutation disease CLINVAR
Entrez Id: 1896
Gene Symbol: EDA
EDA 		0.110 GeneticVariation disease BEFREE The mouse upper second molars in the Eda pathway mutants show the highest incidence of taurodontism, this enhanced susceptibility being matched in human patients with mutations in EDA-A1. 28813629 2017
Entrez Id: 1896
Gene Symbol: EDA
EDA 		0.110 Biomarker disease HPO
Entrez Id: 54084
Gene Symbol: TSPEAR
TSPEAR 		0.100 GeneticVariation disease CLINVAR Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis. 27736875 2016
Entrez Id: 54082
Gene Symbol: TSPEAR-AS1
TSPEAR-AS1 		0.100 GeneticVariation disease CLINVAR Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis. 27736875 2016
Entrez Id: 55505
Gene Symbol: NOP10
NOP10 		0.100 Biomarker disease HPO
Entrez Id: 5073
Gene Symbol: PARN
PARN 		0.100 Biomarker disease HPO
Entrez Id: 51750
Gene Symbol: RTEL1
RTEL1 		0.100 Biomarker disease HPO
Entrez Id: 2314
Gene Symbol: FLII
FLII 		0.100 Biomarker disease HPO
Entrez Id: 57539
Gene Symbol: WDR35
WDR35 		0.100 Biomarker disease HPO
Entrez Id: 57728
Gene Symbol: WDR19
WDR19 		0.100 Biomarker disease HPO
Entrez Id: 80169
Gene Symbol: CTC1
CTC1 		0.100 Biomarker disease HPO
Entrez Id: 4750
Gene Symbol: NEK1
NEK1 		0.100 Biomarker disease HPO
Entrez Id: 4952
Gene Symbol: OCRL
OCRL 		0.100 Biomarker disease HPO
Entrez Id: 2972
Gene Symbol: BRF1
BRF1 		0.100 Biomarker disease HPO
Entrez Id: 55651
Gene Symbol: NHP2
NHP2 		0.100 Biomarker disease HPO
Entrez Id: 7012
Gene Symbol: TERC
TERC 		0.100 Biomarker disease HPO
Entrez Id: 2972
Gene Symbol: BRF1
BRF1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3 		0.100 CausalMutation disease CLINVAR
Entrez Id: 51098
Gene Symbol: IFT52
IFT52 		0.100 Biomarker disease HPO