Activity
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| Fetal anomalies v8.26 | ATXN7L3 | Ida Ertmanska commented on gene: ATXN7L3 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | ATXN7L3 | Natalie Chandler reviewed gene: ATXN7L3: Rating: AMBER; Mode of pathogenicity: ; Publications: 38753057; Phenotypes: Harel-Tora neurodevelopmental syndrome, OMIM:621377, Harel-Tora neurodevelopmental syndrome, MONDO:0980703; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | ATXN7L3 |
Ida Ertmanska gene: ATXN7L3 was added gene: ATXN7L3 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: ATXN7L3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: ATXN7L3 were set to 38753057 Phenotypes for gene: ATXN7L3 were set to Harel-Tora neurodevelopmental syndrome, OMIM:621377; Harel-Tora neurodevelopmental syndrome, MONDO:0980703 |
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