Symbol Name ID |
Myo1h
myosin 1H MGI:1914674 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of temperature regulation |
Disease(s) Associated with MYO1H | |
congenital central hypoventilation syndrome |
Mouse Phenotypes | decreased urine magnesium level |
|
Availability | Mouse Genotype | |
Myo1htm1b(KOMP)Wtsi/Myo1h+ |
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 08/02/2024 MGI 6.24 |
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