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| Short QT syndrome v2.8 | ALG10B | Sarah Leigh Entity copied from Cardiac arrhythmias - previous panel v1.5 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Short QT syndrome v2.8 | ALG10B |
Sarah Leigh gene: ALG10B was added gene: ALG10B was added to Short QT syndrome. Sources: Other Mode of inheritance for gene: ALG10B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ALG10B were set to 15280551 Phenotypes for gene: ALG10B were set to {Acquired long QT syndrome, reduced susceptibility to} OMIM:613688 |
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| Short QT syndrome v2.7 | ALG10 | Sarah Leigh changed review comment from: Not associated with Short QT phenotype in OMIM or in Gen2Phen.; to: ALG10 OMIM:618355 is not associated with Short QT phenotype in OMIM or in Gen2Phen. However, ALG10B OMIM:603313 is associated with Long QT syndrome, acquired, reduced susceptibility to OMIM:613688 (PMID:15280551). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Short QT syndrome v2.7 | ALG10 | Sarah Leigh commented on gene: ALG10: The correct gene name is: ALG10B OMIM:603313 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||