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Symbol Name ID |
Myl1
myosin, light polypeptide 1 MGI:97269 |
| Darker colors indicate more annotations |
| Human Phenotypes | Death in infancy |
| Disease(s) Associated with MYL1 | |
| congenital myopathy 14 |
| Mouse Phenotypes | decreased survivor rate |
embryonic lethality between somite formation and embryo turning, incomplete penetrance |
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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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