Multi-Core Congenital Myopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0270962
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Genes

16 genes associated with the disease Multi-Core Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AICDA activation-induced cytidine deaminase
B3GNT1
CHKB choline kinase beta
FKRP fukutin related protein
FKTN fukutin
ITGA7 integrin, alpha 7
LARGE like-glycosyltransferase
LMNA lamin A/C
MEGF10 multiple EGF-like-domains 10
MYH7 myosin, heavy chain 7, cardiac muscle, beta
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POMT1 protein-O-mannosyltransferase 1
RYR1 ryanodine receptor 1 (skeletal)
SELENON selenoprotein N
TRDN triadin
TTN titin