muscular disease Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A musculoskeletal system disease that affects the muscles. (Human Disease Ontology, DOID_0080000)
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Genes

22 genes associated with the disease muscular disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PHACTR1 phosphatase and actin regulator 1 0.790827
RYR2 ryanodine receptor 2 (cardiac) 0.368757
CELSR2 cadherin, EGF LAG seven-pass G-type receptor 2 0.163718
MRPS6 mitochondrial ribosomal protein S6 0.055232
MIA3 melanoma inhibitory activity family, member 3 0.011006
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 0.010805
CXCL12 chemokine (C-X-C motif) ligand 12 0.010693
WDR12 WD repeat domain 12 0.010659
C12ORF42 chromosome 12 open reading frame 42 0.010401
MARC1 mitochondrial amidoxime reducing component 1 0.010254
RCSD1 RCSD domain containing 1 0.01016
SLC22A3 solute carrier family 22 (organic cation transporter), member 3 0.01012
CLEC14A C-type lectin domain family 14, member A 0.010022
COL4A2 collagen, type IV, alpha 2 0.010022
PPP4R2 protein phosphatase 4, regulatory subunit 2 0.009793
TENM1 teneurin transmembrane protein 1 0.009793
BAG3 BCL2-associated athanogene 3 0.009793
LZTS1 leucine zipper, putative tumor suppressor 1 0.009665
LTA lymphotoxin alpha 0.009665
SETBP1 SET binding protein 1 0.009573
ADAMTS7 ADAM metallopeptidase with thrombospondin type 1 motif, 7 0.009399
ZBTB17 zinc finger and BTB domain containing 17 0.008963