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Fetal anomalies v2.28 PRKACA chirag patel Publications for gene: PRKACA were set to 33058759
Fetal anomalies v2.27 PRKACA chirag patel Phenotypes for gene: PRKACA were changed from Cardioacrofacial dysplasia 1, MONDO:0030876 to Cardioacrofacial dysplasia 1, MONDO:0030876
Fetal anomalies v2.26 PRKACA chirag patel Phenotypes for gene: PRKACA were changed from Cardioacrofacial dysplasia 1-MIM#619142 to Cardioacrofacial dysplasia 1, MONDO:0030876
Fetal anomalies v2.25 chirag patel Added reviews for gene PRKACA from panel Polydactyly
Fetal anomalies v2.0 PRKACA Gene migrated from ENSG00000072062 to ENSG00000072062 (gene set migration)
Fetal anomalies v0.1515 PRKACA Zornitza Stark Marked gene: PRKACA as ready
Fetal anomalies v0.1515 PRKACA Zornitza Stark Gene: prkaca has been classified as Green List (High Evidence).
Fetal anomalies v0.1515 PRKACA Zornitza Stark Classified gene: PRKACA as Green List (high evidence)
Fetal anomalies v0.1515 PRKACA Zornitza Stark Gene: prkaca has been classified as Green List (High Evidence).
Fetal anomalies v0.1469 PRKACA Krithika Murali gene: PRKACA was added
gene: PRKACA was added to Fetal anomalies. Sources: Expert list,Literature
Mode of inheritance for gene: PRKACA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: PRKACA were set to 33058759
Phenotypes for gene: PRKACA were set to Cardioacrofacial dysplasia 1-MIM#619142
Review for gene: PRKACA was set to GREEN
Added comment: Heterozygous variants were identified in affected individuals from 3 unrelated families and associated with cardioacrofacial dysplasia-1 (CAFD1). Phenotype includes congenital cardiac defects (mainly atrium or atrioventricular septal defect), limb anomalies (short limbs, brachydactyly, postaxial polydactyly) and dysmorphic facial features. Fetal phenotype also reported.
Sources: Expert list, Literature