Gene: PARD3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 56288
Gene Symbol: PARD3
PARD3 		0.400 CausalMutation disease CLINVAR Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. 27925688 2017
Entrez Id: 56288
Gene Symbol: PARD3
PARD3 		0.400 SusceptibilityMutation disease CLINVAR Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. 27925688 2017
Entrez Id: 56288
Gene Symbol: PARD3
PARD3 		0.400 GeneticVariation disease UNIPROT Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation. 27925688 2017