Left Ventricular Noncompaction Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1836118
Similar Terms
Downloads & Tools

Genes

35 genes associated with the disease Left Ventricular Noncompaction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ACTC1 actin, alpha, cardiac muscle 1
COA6 cytochrome c oxidase assembly factor 6
DMD dystrophin
DTNA dystrobrevin, alpha
EMD emerin
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LDB3 LIM domain binding 3
LMNA lamin A/C
MIB1 mindbomb E3 ubiquitin protein ligase 1
MIB2 mindbomb E3 ubiquitin protein ligase 2
MIPEP mitochondrial intermediate peptidase
MYBPC3 myosin binding protein C, cardiac
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYH7B myosin, heavy chain 7B, cardiac muscle, beta
NNT nicotinamide nucleotide transhydrogenase
NONO non-POU domain containing, octamer-binding
PKP2 plakophilin 2
PLEKHM2 pleckstrin homology domain containing, family M (with RUN domain) member 2
PRDM16 PR domain containing 16
RYR2 ryanodine receptor 2 (cardiac)
SCN5A sodium channel, voltage gated, type V alpha subunit
SDHA succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
SDHAF1 succinate dehydrogenase complex assembly factor 1
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SKI SKI proto-oncogene
SLC39A8 solute carrier family 39 (zinc transporter), member 8
TAZ tafazzin
TNNT2 troponin T type 2 (cardiac)
TPM1 tropomyosin 1 (alpha)
TRIM8 tripartite motif containing 8
TTN titin
VCL vinculin
YWHAE tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon