| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Dilated Cardiomyopathy v0.50 | DOLK | Zornitza Stark Marked gene: DOLK as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.50 | DOLK | Zornitza Stark Gene: dolk has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.50 | DOLK | Zornitza Stark Classified gene: DOLK as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.50 | DOLK | Zornitza Stark Gene: dolk has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.43 | DOLK |
Paul De Fazio gene: DOLK was added gene: DOLK was added to Dilated Cardiomyopathy. Sources: Literature Mode of inheritance for gene: DOLK was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DOLK were set to 31741824; 28816422; 24144945; 22242004 Phenotypes for gene: DOLK were set to Congenital disorder of glycosylation, type Im MIM#610768 Review for gene: DOLK was set to AMBER gene: DOLK was marked as current diagnostic Added comment: Not curated by ClinGen. This is a CDG gene. Patients may present with DCM (among other phenotypes). PMID 22242004 describes 11 young (5-13) patients with "predominantly nonsyndromic presentation of DCM". Sources: Literature |
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