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Symbol Name ID |
Mymk
myomaker, myoblast fusion factor MGI:1913389 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
Feeding difficulties |
| Disease(s) Associated with MYMK | ||
| Carey-Fineman-Ziter syndrome |
| Mouse Phenotypes | paralysis |
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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 04/16/2024 MGI 6.23 |
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