Activity
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| Fetal anomalies v8.26 | TNNC2 | Ida Ertmanska commented on gene: TNNC2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | TNNC2 | Sarah Graham reviewed gene: TNNC2: Rating: GREEN; Mode of pathogenicity: ; Publications: 40560134, 33755597; Phenotypes: congenital myopathy 15, MONDO:0859335, Congenital myopathy 15, OMIM:620161; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | TNNC2 |
Ida Ertmanska gene: TNNC2 was added gene: TNNC2 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: TNNC2 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal Publications for gene: TNNC2 were set to 40560134; 33755597 Phenotypes for gene: TNNC2 were set to congenital myopathy 15, MONDO:0859335; Congenital myopathy 15, OMIM:620161 |
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