Gene: PRUNE1 ×
Source: INFERRED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1 		0.100 CausalMutation phenotype CLINVAR Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype. 28211990 2017
Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1 		0.100 CausalMutation phenotype CLINVAR PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment. 28334956 2017
Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1 		0.100 CausalMutation phenotype CLINVAR Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease. 26539891 2015
Entrez Id: 58497
Gene Symbol: PRUNE1
PRUNE1 		0.100 CausalMutation phenotype CLINVAR De novo mutations revealed by whole-exome sequencing are strongly associated with autism. 22495306 2012