Gene: PRICKLE1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 144165
Gene Symbol: PRICKLE1
PRICKLE1 		0.020 GeneticVariation disease BEFREE A de novo mutation in PRICKLE1 associated with myoclonic epilepsy and autism spectrum disorder. 29790814 2018
Entrez Id: 144165
Gene Symbol: PRICKLE1
PRICKLE1 		0.020 GeneticVariation disease BEFREE Homozygous recessive mutations in the PRICKLE1 gene were originally reported in three consanguineous families with myoclonic epilepsy. 26727662 2015