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Mendeliome v2.0 ZAR1 Gene migrated from ENSG00000182223 to ENSG00000182223 (gene set migration)
Mendeliome v1.4957 ZAR1 Zornitza Stark Phenotypes for gene: ZAR1 were changed from Multi locus imprinting disturbance in offspring to Premature Ovarian Insufficiency MONDO:0005387, ZAR1-related; Multi locus imprinting disturbance in offspring
Mendeliome v1.4956 ZAR1 Zornitza Stark Mode of inheritance for gene: ZAR1 was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v1.4955 ZAR1 Zornitza Stark Classified gene: ZAR1 as Green List (high evidence)
Mendeliome v1.4955 ZAR1 Zornitza Stark Gene: zar1 has been classified as Green List (High Evidence).
Mendeliome v1.4944 ZAR1 Sangavi Sivagnanasundram reviewed gene: ZAR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 36732629, 35296332; Phenotypes: Multi locus imprinting disturbance in offspring, Premature Ovarian Insufficiency MONDO:0005387, ZAR1-related; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v0.9389 ZAR1 Zornitza Stark Marked gene: ZAR1 as ready
Mendeliome v0.9389 ZAR1 Zornitza Stark Gene: zar1 has been classified as Red List (Low Evidence).
Mendeliome v0.9389 ZAR1 Zornitza Stark gene: ZAR1 was added
gene: ZAR1 was added to Mendeliome. Sources: Expert Review
Mode of inheritance for gene: ZAR1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ZAR1 were set to 29574422; 31598710; 12539046
Phenotypes for gene: ZAR1 were set to Multi locus imprinting disturbance in offspring
Review for gene: ZAR1 was set to RED
Added comment: Single report of biallelic variants in this gene in a mother of a child with Multi locus imprinting disturbance (MLID) with some features of Beckwith Wiedemann Syndrome. Shown to be a maternal effect gene that functions at the oocyte to embryo transition.
Sources: Expert Review