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| Fetal anomalies v8.26 | TSPYL1 | Ida Ertmanska commented on gene: TSPYL1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | TSPYL1 | Sarah Graham reviewed gene: TSPYL1: Rating: AMBER; Mode of pathogenicity: ; Publications: 32885560, 15273283, 33075815, 36082874; Phenotypes: Sudden infant death with dysgenesis of the testes syndrome, OMIM:608800; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | TSPYL1 |
Ida Ertmanska gene: TSPYL1 was added gene: TSPYL1 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: TSPYL1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TSPYL1 were set to 32885560; 15273283; 33075815; 36082874 Phenotypes for gene: TSPYL1 were set to Sudden infant death with dysgenesis of the testes syndrome, OMIM:608800 |
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