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Genetic Epilepsy v2.0 PPFIA3 Gene migrated from ENSG00000177380 to ENSG00000177380 (gene set migration)
Genetic Epilepsy v1.119 PPFIA3 Zornitza Stark Phenotypes for gene: PPFIA3 were changed from Neurodevelopmental disorder, MONDO:0700092, PPFIA3-related to Paul-Chao neurodevelopmental syndrome, MIM# 621122
Genetic Epilepsy v1.118 PPFIA3 Zornitza Stark edited their review of gene: PPFIA3: Changed phenotypes: Paul-Chao neurodevelopmental syndrome, MIM# 621122
Genetic Epilepsy v1.8 PPFIA3 Zornitza Stark Publications for gene: PPFIA3 were set to 38723631
Genetic Epilepsy v1.7 PPFIA3 Zornitza Stark Publications for gene: PPFIA3 were set to 37034625
Genetic Epilepsy v1.6 PPFIA3 Zornitza Stark edited their review of gene: PPFIA3: Changed publications: 38723631
Genetic Epilepsy v0.2146 PPFIA3 Zornitza Stark Marked gene: PPFIA3 as ready
Genetic Epilepsy v0.2146 PPFIA3 Zornitza Stark Gene: ppfia3 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.2146 PPFIA3 Zornitza Stark Classified gene: PPFIA3 as Green List (high evidence)
Genetic Epilepsy v0.2146 PPFIA3 Zornitza Stark Gene: ppfia3 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.2145 PPFIA3 Zornitza Stark gene: PPFIA3 was added
gene: PPFIA3 was added to Genetic Epilepsy. Sources: Literature
Mode of inheritance for gene: PPFIA3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: PPFIA3 were set to 37034625
Phenotypes for gene: PPFIA3 were set to Neurodevelopmental disorder, MONDO:0700092, PPFIA3-related
Review for gene: PPFIA3 was set to GREEN
Added comment: 19 individuals with mono-allelic variants presenting with features including developmental delay, intellectual disability, hypotonia, micro/macrocephaly, autism, and epilepsy. One individual with compound het variants: insufficient evidence for bi-allelic variants causing disease.
Sources: Literature