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Mendeliome v1.459 FRA10AC1 Zornitza Stark Phenotypes for gene: FRA10AC1 were changed from Neurodevelopmental disorder, MONDO:0700092, FRA10AC1-related to Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities, MIM# 620113
Mendeliome v1.458 FRA10AC1 Zornitza Stark edited their review of gene: FRA10AC1: Changed phenotypes: Neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities, MIM# 620113
Mendeliome v0.11557 FRA10AC1 Zornitza Stark Phenotypes for gene: FRA10AC1 were changed from to Neurodevelopmental disorder, MONDO:0700092, FRA10AC1-related
Mendeliome v0.11556 FRA10AC1 Zornitza Stark Publications for gene: FRA10AC1 were set to 15203205
Mendeliome v0.11555 FRA10AC1 Zornitza Stark Mode of inheritance for gene: FRA10AC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.11541 FRA10AC1 Ain Roesley Classified gene: FRA10AC1 as Green List (high evidence)
Mendeliome v0.11541 FRA10AC1 Ain Roesley Gene: fra10ac1 has been classified as Green List (High Evidence).
Mendeliome v0.10835 FRA10AC1 Zornitza Stark changed review comment from: Conclusion of this study was that FRA10A is likely a benign folate-sensitive fragile site.; to: PMID 15203205: Conclusion of this study was that FRA10A is likely a benign folate-sensitive fragile site.
Mendeliome v0.10835 FRA10AC1 Zornitza Stark edited their review of gene: FRA10AC1: Added comment: PMID 34694367: 5 individuals from 3 unrelated families reported.

Variable ID, possibly related to variant type with LoF variants associated with more severe ID. All individuals had microcephaly, hypoplasia or agenesis of the corpus callosum, growth retardation, and craniofacial dysmorphism.; Changed rating: GREEN; Changed publications: 15203205, 34694367; Changed phenotypes: Neurodevelopmental disorder, MONDO:0700092, FRA10AC1-related; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.1330 FRA10AC1 Zornitza Stark Marked gene: FRA10AC1 as ready
Mendeliome v0.1330 FRA10AC1 Zornitza Stark Gene: fra10ac1 has been classified as Red List (Low Evidence).
Mendeliome v0.1330 FRA10AC1 Zornitza Stark Publications for gene: FRA10AC1 were set to
Mendeliome v0.1329 FRA10AC1 Zornitza Stark Classified gene: FRA10AC1 as Red List (low evidence)
Mendeliome v0.1329 FRA10AC1 Zornitza Stark Gene: fra10ac1 has been classified as Red List (Low Evidence).
Mendeliome v0.1328 FRA10AC1 Zornitza Stark reviewed gene: FRA10AC1: Rating: RED; Mode of pathogenicity: None; Publications: 15203205; Phenotypes: ; Mode of inheritance: None
Mendeliome v0.0 FRA10AC1 Zornitza Stark gene: FRA10AC1 was added
gene: FRA10AC1 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: FRA10AC1 was set to Unknown