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| 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 |
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