|
Symbol Name ID |
Usp9x
ubiquitin specific peptidase 9, X chromosome MGI:894681 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dandy-Walker malformation |
Ventriculomegaly |
Abnormal cortical gyration |
Hypoplasia of the corpus callosum |
Cerebellar hypoplasia |
Delayed speech and language development |
Autistic behavior |
Aggressive behavior |
Compulsive behaviors |
Intellectual disability |
Global developmental delay |
Seizure |
| Disease(s) Associated with USP9X | ||||||||||||
| female-restricted syndromic X-linked intellectual disability 99 | ||||||||||||
| non-syndromic X-linked intellectual disability 99 |
| Mouse Phenotypes | open neural tube |
|
| Availability | Mouse Genotype | |
| Usp9xGt(XK141)Byg/Y | ||
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 |
|
|
|
||
Analysis Tools