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Symbol Name ID |
Mymk
myomaker, myoblast fusion factor MGI:1913389 |
| 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 MYMK | ||||||||||||
| Carey-Fineman-Ziter syndrome |
| Mouse Phenotypes | abnormal myoblast differentiation |
abnormal myoblast fusion |
abnormal muscle development |
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| Availability | Mouse Genotype | |||
| Mymktm1e(KOMP)Wtsi/Mymktm1e(KOMP)Wtsi | ||||
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 04/09/2024 MGI 6.23 |
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