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| Cardiomyopathy_Paediatric v1.320 | TTN | Zornitza Stark Marked gene: TTN as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.320 | TTN | Zornitza Stark Gene: ttn has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.320 | TTN | Zornitza Stark Publications for gene: TTN were set to http://www.ncbi.nlm.nih.gov/pubmed/22335739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.319 | TTN | Zornitza Stark reviewed gene: TTN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: dilated cardiomyopathy 1G MONDO:0011400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.105 | TTN |
Sarah Milton Source South West GLH was removed from TTN. Source NHS GMS was removed from TTN. Source ClinGen was added to TTN. Phenotypes for gene: TTN were changed from Cardiomyopathy, familial hypertrophic, 9,; Cardiomyopathy, dilated, 1G to Dilated cardiomyopathy 1G, MONDO:0011400; Hypertrophic cardiomyopathy, MONDO:0005045 |
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| Cardiomyopathy_Paediatric v1.0 | TTN | Gene migrated from ENSG00000155657 to ENSG00000155657 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v0.0 | TTN |
Zornitza Stark gene: TTN was added gene: TTN was added to Cardiomyopathy_Paediatric. Sources: NHS GMS,South West GLH,Expert Review Green Mode of inheritance for gene: TTN was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TTN were set to http://www.ncbi.nlm.nih.gov/pubmed/22335739 Phenotypes for gene: TTN were set to Cardiomyopathy, familial hypertrophic, 9,; Cardiomyopathy, dilated, 1G |
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