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Congenital Heart Defect v1.0 PLD1 Gene migrated from ENSG00000075651 to ENSG00000075651 (gene set migration)
Congenital Heart Defect v0.91 PLD1 Zornitza Stark Tag founder tag was added to gene: PLD1.
Congenital Heart Defect v0.91 PLD1 Zornitza Stark Phenotypes for gene: PLD1 were changed from Cardiac valvular defect, developmental, MIM# 212093 to Cardiac valvular defect, developmental, MIM# 212093; neonatal cardiomyopathy
Congenital Heart Defect v0.90 PLD1 Zornitza Stark Publications for gene: PLD1 were set to 27799408
Congenital Heart Defect v0.89 PLD1 Zornitza Stark Classified gene: PLD1 as Green List (high evidence)
Congenital Heart Defect v0.89 PLD1 Zornitza Stark Gene: pld1 has been classified as Green List (High Evidence).
Congenital Heart Defect v0.88 PLD1 Zornitza Stark edited their review of gene: PLD1: Added comment: PMID 33645542: 31 individuals from 20 families reported, presenting predominantly with congenital cardiac valve defects and some with neonatal cardiomyopathy. p.I668F is a founder variant among Ashkenazi Jews (allele frequency of ~2%).; Changed rating: GREEN; Changed publications: 27799408, 33645542; Changed phenotypes: Cardiac valvular defect, developmental, MIM# 212093
Congenital Heart Defect v0.11 PLD1 Zornitza Stark Marked gene: PLD1 as ready
Congenital Heart Defect v0.11 PLD1 Zornitza Stark Gene: pld1 has been classified as Amber List (Moderate Evidence).
Congenital Heart Defect v0.11 PLD1 Zornitza Stark Classified gene: PLD1 as Amber List (moderate evidence)
Congenital Heart Defect v0.11 PLD1 Zornitza Stark Gene: pld1 has been classified as Amber List (Moderate Evidence).
Congenital Heart Defect v0.10 PLD1 Zornitza Stark gene: PLD1 was added
gene: PLD1 was added to Congenital Heart Defect. Sources: Expert list
Mode of inheritance for gene: PLD1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PLD1 were set to 27799408
Phenotypes for gene: PLD1 were set to Cardiac valvular defect, developmental, MIM# 212093
Review for gene: PLD1 was set to AMBER
Added comment: Four individuals from two families reported.
Sources: Expert list