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Browse result for Myopathy

※ introduction

    In medicine, myopathy is a disease of the muscle in which the muscle fibers do not function properly. Myopathy means muscle disease (Greek : myo- muscle + patheia -pathy : suffering). This meaning implies that the primary defect is within the muscle, as opposed to the nerves ("neuropathies" or "neurogenic" disorders) or elsewhere (e.g., the brain). This muscular defect typically results in myalgia (muscle pain), muscle weakness (reduced muscle force), or premature muscle fatigue (initially normal, but declining muscle force). Muscle cramps, stiffness, spasm, and contracture can also be associated with myopathy. Myopathy experienced over a long period (chronic) may result in the muscle becoming an abnormal size, such as muscle atrophy (abnormally small) or a pseudoathletic appearance (abnormally large). Capture myopathy can occur in wild or captive animals, such as deer and kangaroos, and leads to morbidity and mortality. It usually occurs as a result of stress and physical exertion during capture and restraint. Muscular disease can be classified as neuromuscular or musculoskeletal in nature. Some conditions, such as myositis, can be considered both neuromuscular and musculoskeletal. Different myopathies may be inherited, infectious, non-communicable, or idiopathic (cause unknown). The disease may be isolated to affecting only muscle (pure myopathy), or may be part of a systemic disease as is typical in mitochondrial myopathies.

Reference
Wiki: Myopathy



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01049O958179531
BAG3
BAG family molecular chaperone regulator 3
Homo sapiens
PTMD00824Q9UKX24620
MYH2
Myosin-2
Homo sapiens
PTMD01405O00499274
BIN1
Myc box-dependent-interacting protein 1
Homo sapiens
PTMD01536P176611674
DES
Desmin
Homo sapiens
PTMD01695P6813358
ACTA1
Actin, alpha skeletal muscle [Cleaved into: Actin, alpha skeletal muscle, intermediate form]
Homo sapiens
PTMD01845Q8WZ427273
TTN
Titin
Homo sapiens
PTMD03660P021444151
MB
Myoglobin
Homo sapiens
PTMD04130P128834625
MYH7
Myosin-7
Homo sapiens
PTMD04823P31415844
CASQ1
Calsequestrin-1
Homo sapiens
PTMD04944P3560988
ACTN2
Alpha-actinin-2
Homo sapiens
PTMD05389P505701785
DNM2
Dynamin-2
Homo sapiens
PTMD05650P557892671
GFER
FAD-linked sulfhydryl oxidase ALR
Homo sapiens
PTMD05675P56539859
CAV3
Caveolin-3
Homo sapiens
PTMD06563Q134964534
MTM1
Myotubularin
Homo sapiens
PTMD06586Q135866786
STIM1
Stromal interaction molecule 1
Homo sapiens
PTMD06608Q136422273
FHL1
Four and a half LIM domains protein 1
Homo sapiens
PTMD06724Q143152318
FLNC
Filamin-C
Homo sapiens
PTMD09968Q8NCE264419
MTMR14
Myotubularin-related protein 14
Homo sapiens
PTMD11211Q96F2519985
ALG14
UDP-N-acetylglucosamine transferase subunit ALG14
Homo sapiens
PTMD11433Q96KG784466
MEGF10
Multiple epidermal growth factor-like domains protein 10
Homo sapiens
PTMD13719Q9NYL251776
MAP3K20
Mitogen-activated protein kinase kinase kinase 20
Homo sapiens
PTMD13989Q9UBF99499
MYOT
Myotilin
Homo sapiens
PTMD14152Q9UHP923676
SMPX
Small muscular protein
Homo sapiens
PTMD14594Q9Y22310020
GNE
Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase [Includes: UDP-N-acetylglucosamine 2-epimerase ; N-acetylmannosamine kinase ]
Homo sapiens
PTMD14733Q9Y2Z451067
YARS2
Tyrosine--tRNA ligase, mitochondrial
Homo sapiens