Symbol Name ID |
Myl9
myosin, light polypeptide 9, regulatory MGI:2138915 |
Darker colors indicate more annotations |
Human Phenotypes | Aganglionic megacolon |
Microcolon |
Megaduodenum |
Thinning of outer muscular layer of small bowel |
Intestinal malrotation |
Intestinal pseudo-obstruction |
Constipation |
Diarrhea |
Nausea and vomiting |
Vomiting |
Dysphagia |
Hypoperistalsis |
Abnormality of the gastrointestinal tract |
Disease(s) Associated with MYL9 | |||||||||||||
megacystis-microcolon-intestinal hypoperistalsis syndrome |
Mouse Phenotypes | abnormal intestine morphology |
distended duodenum |
abnormal jejunum morphology |
distended jejunum |
abnormal intestinal peristalsis |
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Availability | Mouse Genotype | |||||
Myl9tm1.1Mzhu/Myl9tm1.1Mzhu | ||||||
Myl9tm1Mzhu/Myl9tm1Mzhu Tg(Acta2-cre)#Xya/0 (conditional) |
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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