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Symbol Name ID |
Myh7
myosin, heavy polypeptide 7, cardiac muscle, beta MGI:2155600 |
| Darker colors indicate more annotations |
| Human Phenotypes | Facial palsy |
Calf muscle hypertrophy |
Calf muscle pseudohypertrophy |
Amyotrophy of ankle musculature |
Toe extensor amyotrophy |
Distal lower limb muscle weakness |
Weakness of long finger extensor muscles |
Scapular winging |
Shoulder girdle muscle weakness |
Shoulder girdle muscle atrophy |
Limb-girdle muscle weakness |
Pelvic girdle muscle weakness |
EMG: myopathic abnormalities |
EMG: neuropathic changes |
Difficulty climbing stairs |
Difficulty running |
Difficulty walking |
Muscle weakness |
Distal muscle weakness |
Generalized muscle weakness |
Neck muscle weakness |
Neck flexor weakness |
Proximal muscle weakness |
Scapuloperoneal weakness |
Type 1 muscle fiber predominance |
Centrally nucleated skeletal muscle fibers |
Muscle fiber hyaline bodies |
Ragged-red muscle fibers |
Rimmed vacuoles |
Tibialis anterior muscle atrophy |
Generalized limb muscle atrophy |
Proximal amyotrophy |
Scapuloperoneal amyotrophy |
Myopathy |
| Disease(s) Associated with MYH7 | ||||||||||||||||||||||||||||||||||
| autosomal dominant hyaline body myopathy | ||||||||||||||||||||||||||||||||||
| autosomal recessive hyaline body myopathy | ||||||||||||||||||||||||||||||||||
| distal myopathy 1 |
| Mouse Phenotypes | decreased cardiac muscle contractility |
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| Availability | Mouse Genotype | |
| Tg(Myh6-Myh7)102Rbns/Tg(Myh6-Myh7)102Rbns | ||
| Tg(Myh6-Myh7)137Rbns/0 | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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