Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.720 Biomarker disease BEFREE However, HYD-1 (Lys-Ile-Lys-Met-Val-Ile-Ser-Trp-Lys-Gly), an integrin antagonist, inhibited the KGF-enhanced epithelial adhesion and rete peg elongation. 28732179 2017
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.720 Biomarker disease GENOMICS_ENGLAND Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies. 25565750 2014
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.720 Biomarker disease BEFREE Genes affecting early tooth development (PAX9, MSX1, and AXIN2) are associated with familial tooth agenesis or oligodontia. 17552940 2007
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.720 GeneticVariation disease UNIPROT The role of MSX1 in human tooth agenesis. 12097313 2002
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.720 GeneticVariation disease UNIPROT We demonstrate that a mutation in the homeobox gene, MSX1, causes a common developmental anomaly, familial tooth agenesis. 8696335 1996
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.720 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.720 Biomarker disease CTD_human
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.720 CausalMutation disease CLINVAR
Entrez Id: 4054
Gene Symbol: LTBP3
LTBP3 		0.300 Biomarker disease CTD_human New recessive truncating mutation in LTBP3 in a family with oligodontia, short stature, and mitral valve prolapse. 25899461 2015
Entrez Id: 10265
Gene Symbol: IRX5
IRX5 		0.300 Biomarker disease CTD_human Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1. 22581230 2012
Entrez Id: 4054
Gene Symbol: LTBP3
LTBP3 		0.300 Biomarker disease CTD_human Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3. 19344874 2009
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.100 GeneticVariation disease GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
Entrez Id: 779
Gene Symbol: CACNA1S
CACNA1S 		0.100 GeneticVariation disease GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
Entrez Id: 25926
Gene Symbol: NOL11
NOL11 		0.100 GeneticVariation disease GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.100 GeneticVariation disease GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15 		0.100 GeneticVariation disease GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
Entrez Id: 5083
Gene Symbol: PAX9
PAX9 		0.020 GeneticVariation disease BEFREE Novel missense mutation in PAX9 gene associated with familial tooth agenesis. 22747565 2013
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2 		0.020 Biomarker disease BEFREE Genes affecting early tooth development (PAX9, MSX1, and AXIN2) are associated with familial tooth agenesis or oligodontia. 17552940 2007
Entrez Id: 5083
Gene Symbol: PAX9
PAX9 		0.020 GeneticVariation disease BEFREE In humans, mutations in PAX9 are associated with unique phenotypes of familial tooth agenesis that mainly involve posterior teeth. 14607846 2004
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2 		0.020 GeneticVariation disease BEFREE Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. 15042511 2004