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Symbol Name ID |
Myl1
myosin, light polypeptide 1 MGI:97269 |
| Darker colors indicate more annotations |
| Human Phenotypes | Polyhydramnios |
Decreased fetal movement |
| Disease(s) Associated with MYL1 | ||
| congenital myopathy 14 |
| Mouse Phenotypes | embryonic growth arrest |
decreased embryo size |
absent mesoderm |
failure of primitive streak formation |
abnormal visceral yolk sac cavity morphology |
abnormal extraembryonic endoderm formation |
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| Availability | Mouse Genotype | ||||||
| Myl1tm1Nros/Myl1tm1Nros | |||||||
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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