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Molecular autopsy

Gene: PRDM16

Red List (low evidence)
PRDM16 (PR/SET domain 16)
EnsemblGeneIds (GRCh38): ENSG00000142611
EnsemblGeneIds (GRCh37): ENSG00000142611
OMIM: 605557, Gene2Phenotype
PRDM16 is in 3 panels

1 review

Ellen McDonagh (Genomics England Curator)

I don't know

This gene was part of an initial gene list collated by Matthew Edwards Royal Brompton Hospital sent 16th Jan 2019 on behalf of the London South GLH for review by the GMS Cardiology Specialist Group. Only gene symbol from the Royal Brompton gene panel was provided - suggested initial gene rating and evidence for inclusion not provided with the list.
Created: 20 Feb 2019, 2:17 p.m.
Created: 20 Feb 2019, 2:17 p.m.

Panel version: 0.86

Details

Mode of Inheritance
Unknown
Sources
  • London South GLH
  • Expert Review Red
Phenotypes
  • Left ventricular noncompaction 8
  • Cardiomyopathy, dilated, 1LL
OMIM
605557
Clinvar variants
Variants in PRDM16
Penetrance
None
Panels with this gene

History Filter Activity

20 Feb 2019, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

Source London South GLH was added to PRDM16.

20 Dec 2018, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: PRDM16 was added gene: PRDM16 was added to Molecular autopsy. Sources: Expert Review Red Mode of inheritance for gene: PRDM16 was set to Unknown Phenotypes for gene: PRDM16 were set to Left ventricular noncompaction 8; Cardiomyopathy, dilated, 1LL