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  3. PRDM16
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Transplant Co-Morbidity Superpanel

Gene: PRDM16

Green List (high evidence)
PRDM16 (PR/SET domain 16)
EnsemblGeneIds (GRCh38): ENSG00000142611
EnsemblGeneIds (GRCh37): ENSG00000142611
OMIM: 605557, Gene2Phenotype
PRDM16 is in 6 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Left ventricular noncompaction 8 MIM#615373
  • Cardiomyopathy, dilated, 1LL MIM#615373
OMIM
605557
Clinvar variants
Variants in PRDM16
Penetrance
None
Publications
Panels with this gene

History Filter Activity

1 Aug 2023, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Bryony Thompson (Royal Melbourne Hospital)

gene: PRDM16 was added gene: PRDM16 was added to Transplant Co-Morbidity Superpanel. Sources: Literature,Expert Review Green Mode of inheritance for gene: PRDM16 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: PRDM16 were set to 34540771; 34935411; 29367541; 24387995; 32183154; 33500567; 33082984; 34350506; 31965688; 29447731; PMID: 23768516; 30847666 Phenotypes for gene: PRDM16 were set to Left ventricular noncompaction 8 MIM#615373; Cardiomyopathy, dilated, 1LL MIM#615373