※ PTMD 2.0 database Online Browse Options
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
Reference
Wiki: Myopathy
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01049 | O95817 | 9531 | BAG3 | BAG family molecular chaperone regulator 3 | Homo sapiens |
| PTMD00824 | Q9UKX2 | 4620 | MYH2 | Myosin-2 | Homo sapiens |
| PTMD01405 | O00499 | 274 | BIN1 | Myc box-dependent-interacting protein 1 | Homo sapiens |
| PTMD01536 | P17661 | 1674 | DES | Desmin | Homo sapiens |
| PTMD01695 | P68133 | 58 | ACTA1 | Actin, alpha skeletal muscle [Cleaved into: Actin, alpha skeletal muscle, intermediate form] | Homo sapiens |
| PTMD01845 | Q8WZ42 | 7273 | TTN | Titin | Homo sapiens |
| PTMD03660 | P02144 | 4151 | MB | Myoglobin | Homo sapiens |
| PTMD04130 | P12883 | 4625 | MYH7 | Myosin-7 | Homo sapiens |
| PTMD04823 | P31415 | 844 | CASQ1 | Calsequestrin-1 | Homo sapiens |
| PTMD04944 | P35609 | 88 | ACTN2 | Alpha-actinin-2 | Homo sapiens |
| PTMD05389 | P50570 | 1785 | DNM2 | Dynamin-2 | Homo sapiens |
| PTMD05650 | P55789 | 2671 | GFER | FAD-linked sulfhydryl oxidase ALR | Homo sapiens |
| PTMD05675 | P56539 | 859 | CAV3 | Caveolin-3 | Homo sapiens |
| PTMD06563 | Q13496 | 4534 | MTM1 | Myotubularin | Homo sapiens |
| PTMD06586 | Q13586 | 6786 | STIM1 | Stromal interaction molecule 1 | Homo sapiens |
| PTMD06608 | Q13642 | 2273 | FHL1 | Four and a half LIM domains protein 1 | Homo sapiens |
| PTMD06724 | Q14315 | 2318 | FLNC | Filamin-C | Homo sapiens |
| PTMD09968 | Q8NCE2 | 64419 | MTMR14 | Myotubularin-related protein 14 | Homo sapiens |
| PTMD11211 | Q96F25 | 19985 | ALG14 | UDP-N-acetylglucosamine transferase subunit ALG14 | Homo sapiens |
| PTMD11433 | Q96KG7 | 84466 | MEGF10 | Multiple epidermal growth factor-like domains protein 10 | Homo sapiens |
| PTMD13719 | Q9NYL2 | 51776 | MAP3K20 | Mitogen-activated protein kinase kinase kinase 20 | Homo sapiens |
| PTMD13989 | Q9UBF9 | 9499 | MYOT | Myotilin | Homo sapiens |
| PTMD14152 | Q9UHP9 | 23676 | SMPX | Small muscular protein | Homo sapiens |
| PTMD14594 | Q9Y223 | 10020 | GNE | Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase [Includes: UDP-N-acetylglucosamine 2-epimerase ; N-acetylmannosamine kinase ] | Homo sapiens |
| PTMD14733 | Q9Y2Z4 | 51067 | YARS2 | Tyrosine--tRNA ligase, mitochondrial | Homo sapiens |
