| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Cardiomyopathy_Paediatric v1.57 | C10orf71 | Sarah Milton Classified gene: C10orf71 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.57 | C10orf71 | Sarah Milton Gene: c10orf71 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Cardiomyopathy_Paediatric v1.56 | C10orf71 |
Sarah Milton gene: C10orf71 was added gene: C10orf71 was added to Cardiomyopathy_Paediatric. Sources: Literature Mode of inheritance for gene: C10orf71 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: C10orf71 were set to 38950288 Phenotypes for gene: C10orf71 were set to Cardiomyopathy, dilated, 1QQ, MIM# 621251 Review for gene: C10orf71 was set to GREEN Added comment: Loss of function variants in C10ORF71 have been associated with adult onset dilated cardiomyopathy, PMID 38950288 reports 3 cases of paediatric onset DCM ages 7-12 from 3 separate families. Sources: Literature |
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