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Symbol Name ID |
Myl9
myosin, light polypeptide 9, regulatory MGI:2138915 |
| Darker colors indicate more annotations |
| Human Phenotypes | Gastroparesis |
| Disease(s) Associated with MYL9 | |
| megacystis-microcolon-intestinal hypoperistalsis syndrome |
| Mouse Phenotypes | abnormal aorta smooth muscle morphology |
abnormal vascular smooth muscle physiology |
abnormal intestinal peristalsis |
impaired smooth muscle contractility |
impaired contractility of jejunal smooth muscle |
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| Availability | Mouse Genotype | |||||
| Myl9tm1Mzhu/Myl9tm1Mzhu Tg(Acta2-cre)#Xya/0 (conditional) |
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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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