Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 154288
Gene Symbol: KHDC3L
KHDC3L
0.020 GeneticVariation disease BEFREE In this study, we have screened NLRP7 and KHDC3L mutations in five patients with recurrent moles and five with sporadic moles. 31220306 2019
Entrez Id: 154288
Gene Symbol: KHDC3L
KHDC3L
0.020 GeneticVariation disease BEFREE However, it is unknown if correct parental origin of every imprinted gene is crucial for normal early differentiation or if abnormal parental imprinting of only one, or some, gene(s) can cause the mole phenotype.Two conceptuses included in the Danish Mole Project stood out since they presented with vesicular chorionic villi and without signs of fetal differentiation, and had apparently biparental diploid genomes, and no mutations in NLRP7 or KHDC3L were detected in the mothers. 26554776 2015