Hernia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0019270
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Genes

27 genes associated with the disease Hernia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
ATP7A ATPase, Cu++ transporting, alpha polypeptide
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
COL2A1 collagen, type II, alpha 1
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
DMPK dystrophia myotonica-protein kinase
DVL1 dishevelled segment polarity protein 1
DVL3 dishevelled segment polarity protein 3
EHMT1 euchromatic histone-lysine N-methyltransferase 1
FANCB Fanconi anemia, complementation group B
FZD2 frizzled class receptor 2
LAMC2 laminin, gamma 2
MECP2 methyl CpG binding protein 2
MVD mevalonate (diphospho) decarboxylase
MYH7 myosin, heavy chain 7, cardiac muscle, beta
NLRP3 NLR family, pyrin domain containing 3
PTDSS1 phosphatidylserine synthase 1
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
SMAD4 SMAD family member 4
TBX1 T-box 1
TBX3 T-box 3
TRIP11 thyroid hormone receptor interactor 11
WNT5A wingless-type MMTV integration site family, member 5A
ZEB1 zinc finger E-box binding homeobox 1