Gene: WNT10B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation. 29384555 2020
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE A classification system for split-hand/ foot malformation (SHFM): A proposal based on 3 pedigrees with WNT10B mutations. 31421290 2020
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE WNT10B variants in split hand/foot malformation: Report of three novel families and review of the literature. 31050392 2019
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE Split hand-foot malformation and a novel WNT10B mutation. 29427788 2018
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE Although six different loci/mutations (SHFM1-SHFM6) have been found from studies on families with SHFM, the causes and associated pathogenic mechanisms for a large number of patients remain unidentified. 28324176 2018
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families. 24211389 2014
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE Investigating linkage to known autosomal SHFM loci mapped the family to SHFM6 locus on chromosome 12p11.1-q13.13. 21554266 2012
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE By examining WNT10B in a patient with sporadic SHFM, we identified a homozygous 4-bp duplication resulting in a premature termination codon. 20635353 2010
Entrez Id: 7480
Gene Symbol: WNT10B
WNT10B 		0.090 GeneticVariation disease BEFREE This is the first reported WNT10b mutation on the pathogenesis of limb development and recessive mutation in SHFM. 18515319 2008