Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease BEFREE With the notable exception of WNT10A (Tooth agenesis, selective, 4, MIM #150400), the genotype-phenotype relationships described in the present cohort represent an expansion of the clinical spectrum associated with these genes: TSPEAR (Deafness, autosomal recessive 98, MIM #614861), LAMB3 (Amelogenesis imperfecta, type IA, MIM #104530; Epidermolysis bullosa, junctional, MIMs #226700 and #226650), and BCOR (Microphthalmia, syndromic 2, MIM #300166). 30046887 2018
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis. 28981473 2017
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease UNIPROT Role of WNT10A in failure of tooth development in humans and zebrafish. 29178643 2017
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease UNIPROT Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients. 27657131 2016
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies. 25545742 2015
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds. 25629078 2015
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease UNIPROT WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations. 24449199 2014
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease UNIPROT WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity. 24311251 2014
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Variability in dentofacial phenotypes in four families with WNT10A mutations. 24398796 2014
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review. 24702986 2014
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome. 24902757 2014
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Late diagnosis of ectodermal dysplasia syndrome. 22670871 2013
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis. 23167694 2013
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease UNIPROT Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia. 23401279 2013
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease UNIPROT Mutations in WNT10A are present in more than half of isolated hypodontia cases. 22581971 2012
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease UNIPROT Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases. 20979233 2011
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum. 21143469 2011
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases. 20979233 2011
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease UNIPROT WNT10A and isolated hypodontia. 21484994 2011
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR Phenotypic variability associated with WNT10A nonsense mutations. 20163410 2010
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome. 19471313 2009
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 GeneticVariation disease CLINVAR WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. 19559398 2009
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 CausalMutation disease CLINVAR WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. 19559398 2009
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A 		0.610 Biomarker disease CTD_human