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Symbol Name ID |
Mymx
myomixer, myoblast fusion factor MGI:3649059 |
| Darker colors indicate more annotations |
| Human Phenotypes | Weakness of facial musculature |
Facial palsy |
Pectoralis hypoplasia |
Flexion contracture |
Hypotonia |
Generalized hypotonia |
Severe muscular hypotonia |
Distal muscle weakness |
Proximal muscle weakness |
Hypoplasia of the musculature |
Skeletal muscle atrophy |
Myopathy |
| Disease(s) Associated with MYMX | ||||||||||||
| Carey-Fineman-Ziter syndrome |
| Mouse Phenotypes | abnormal myoblast fusion |
abnormal limb muscle morphology |
abnormal muscle morphology |
abnormal skeletal muscle morphology |
abnormal intercostal muscle morphology |
muscle weakness |
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| Availability | Mouse Genotype | ||||||
| Mymxem1Shcs/Mymxem1Shcs | |||||||
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 04/23/2024 MGI 6.23 |
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