death, sudden, cardiac Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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27 genes associated with the disease death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACYP2 acylphosphatase 2, muscle type
AP1G2 adaptor-related protein complex 1, gamma 2 subunit
ARL5B ADP-ribosylation factor-like 5B
ATF1 activating transcription factor 1
BAZ2B bromodomain adjacent to zinc finger domain, 2B
CDH4 cadherin 4, type 1, R-cadherin (retinal)
CHL1 cell adhesion molecule L1-like
CHRNB4 cholinergic receptor, nicotinic, beta 4 (neuronal)
CLSTN2 calsyntenin 2
DEGS2 delta(4)-desaturase, sphingolipid 2
ESR1 estrogen receptor 1
GALNT13 polypeptide N-acetylgalactosaminyltransferase 13
GRIA1 glutamate receptor, ionotropic, AMPA 1
KCTD1 potassium channel tetramerization domain containing 1
MAML2 mastermind-like 2 (Drosophila)
MARCH8 membrane-associated ring finger (C3HC4) 8, E3 ubiquitin protein ligase
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
OCM2 oncomodulin 2
PARP4 poly (ADP-ribose) polymerase family, member 4
PLCE1 phospholipase C, epsilon 1
RAP1GAP2 RAP1 GTPase activating protein 2
RSPH6A radial spoke head 6 homolog A (Chlamydomonas)
SIN3A SIN3 transcription regulator family member A
TANC1 tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1
TMEFF2 transmembrane protein with EGF-like and two follistatin-like domains 2
ZNF385B zinc finger protein 385B