Symbol Name ID |
Myl9
myosin, light polypeptide 9, regulatory MGI:2138915 |
Darker colors indicate more annotations |
Human Phenotypes | Abdominal distention |
Omphalocele |
Umbilical hernia |
Disease(s) Associated with MYL9 | |||
megacystis-microcolon-intestinal hypoperistalsis syndrome |
Mouse Phenotypes | decreased body size |
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Availability | Mouse Genotype | |
Myl9tm1.1Mzhu/Myl9tm1.1Mzhu |
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 04/30/2024 MGI 6.23 |
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