Gene: PRDM16 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 63976
Gene Symbol: PRDM16
PRDM16 		0.320 Biomarker disease BEFREE PRDM16 was recently identified as a causative gene of left ventricular non-compaction and dilated cardiomyopathy in 1p36 deletion syndrome, which is characterized by heart failure, arrhythmia and sudden cardiac death. 25035420 2014
Entrez Id: 63976
Gene Symbol: PRDM16
PRDM16 		0.320 GeneticVariation disease BEFREE In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM. 23768516 2013
Entrez Id: 63976
Gene Symbol: PRDM16
PRDM16 		0.320 ChromosomalRearrangement disease ORPHANET In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM. 23768516 2013