Muscle Degeneration Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description pathological deterioration of muscle tissue, often accompanied by loss of function (Mammalian Phenotype Ontology, MP_0000749)
External Link https://www.disgenet.org/browser/0/1/0/C0234958
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
AR androgen receptor
ARIH2 ariadne RBR E3 ubiquitin protein ligase 2
ATP2A1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
BHLHE40 basic helix-loop-helix family, member e40
BMP2 bone morphogenetic protein 2
CAPN3 calpain 3, (p94)
CCT3 chaperonin containing TCP1, subunit 3 (gamma)
CENPX centromere protein X
CISD2 CDGSH iron sulfur domain 2
CLP1 cleavage and polyadenylation factor I subunit 1
CLU clusterin
CNNM1 cyclin and CBS domain divalent metal cation transport mediator 1
COLEC12 collectin sub-family member 12
CRMP1 collapsin response mediator protein 1
CTF1 cardiotrophin 1
DAG1 dystroglycan 1 (dystrophin-associated glycoprotein 1)
DAPK2 death-associated protein kinase 2
DENR density-regulated protein
DES desmin
DMD dystrophin
DNAH8 dynein, axonemal, heavy chain 8
DNM1L dynamin 1-like
DUX4 double homeobox 4
DYSF dysferlin
FHL1 four and a half LIM domains 1
FKRP fukutin related protein
FKTN fukutin
FRG1 FSHD region gene 1
GAA glucosidase, alpha; acid
GPR180 G protein-coupled receptor 180
HEXIM1 hexamethylene bis-acetamide inducible 1
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
IL10 interleukin 10
ITGAM integrin, alpha M (complement component 3 receptor 3 subunit)
MB myoglobin
MME membrane metallo-endopeptidase
MSTN myostatin
MUL1 mitochondrial E3 ubiquitin protein ligase 1
MYH2 myosin, heavy chain 2, skeletal muscle, adult
MYOT myotilin
NOTCH3 notch 3
OPA1 optic atrophy 1 (autosomal dominant)
PABPN1 poly(A) binding protein, nuclear 1
PANX1 pannexin 1
PANX3 pannexin 3
PARK2 parkin RBR E3 ubiquitin protein ligase
PARP1 poly (ADP-ribose) polymerase 1
PAX7 paired box 7
PINK1 PTEN induced putative kinase 1
PPID peptidylprolyl isomerase D
PPIF peptidylprolyl isomerase F
PTRH2 peptidyl-tRNA hydrolase 2
RET ret proto-oncogene
RGS12 regulator of G-protein signaling 12
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SIL1 SIL1 nucleotide exchange factor
SOD1 superoxide dismutase 1, soluble
STIM1 stromal interaction molecule 1
TARDBP TAR DNA binding protein
TBP TATA box binding protein
TBPL1 TBP-like 1
TRPV2 transient receptor potential cation channel, subfamily V, member 2
TYRP1 tyrosinase-related protein 1
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
UTRN utrophin
ZNF645 zinc finger protein 645