Symbol Name ID |
Myo1h
myosin 1H MGI:1914674 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Disease(s) Associated with MYO1H | |
congenital central hypoventilation syndrome |
Mouse Phenotypes | abnormal motor coordination/balance |
|
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) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|