abnormality of the calf musculature Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001430
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Genes

18 genes associated with the abnormality of the calf musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANO5 anoctamin 5
AR androgen receptor
CAV3 caveolin 3
DES desmin
DMD dystrophin
FBN2 fibrillin 2
FKRP fukutin related protein
FKTN fukutin
FLNC filamin C, gamma
LMNA lamin A/C
MYH7 myosin, heavy chain 7, cardiac muscle, beta
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
TCAP titin-cap
TRIM32 tripartite motif containing 32
TRPV4 transient receptor potential cation channel, subfamily V, member 4
TTN titin