Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4038
Gene Symbol: LRP4
LRP4
0.030 GeneticVariation disease BEFREE This recessive mutation in LRP4 confirmed the diagnosis of CLS syndrome in two patients present with isolated hand syndactyly. 30041615 2018
Entrez Id: 4038
Gene Symbol: LRP4
LRP4
0.030 GeneticVariation disease BEFREE CLS was recently associated with mutations in the low-density lipoprotein receptor-related protein 4 (LRP4) gene and dysregulated canonical WNT signaling. 23664847 2013
Entrez Id: 4038
Gene Symbol: LRP4
LRP4
0.030 GeneticVariation disease BEFREE By sequencing candidate genes, we identified recessive LRP4 mutations in 12 families with CLS. 20381006 2010