Symbol Name ID |
Myo5b
myosin VB MGI:106598 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hepatomegaly |
Abdominal distention |
Short stature |
Failure to thrive |
Growth delay |
Disease(s) Associated with MYO5B | ||||||
microvillus inclusion disease | ||||||
progressive familial intrahepatic cholestasis |
Mouse Phenotypes | decreased body weight |
weight loss |
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Availability | Mouse Genotype | ||
Myo5btm1a(KOMP)Wtsi/Myo5btm1a(KOMP)Wtsi | |||
Myo5btm1.1Cle/Myo5btm1.1Cle Tg(Vil1-cre/ERT2)23Syr/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 03/19/2024 MGI 6.23 |
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