|
Symbol Name ID |
Hax1
HCLS1 associated X-1 MGI:1346319 |
| Darker colors indicate more annotations |
| Human Phenotypes | Clumsiness |
Intellectual disability |
Global developmental delay |
Seizure |
Impaired vibratory sensation |
| Disease(s) Associated with HAX1 | |||||
| severe congenital neutropenia 3 |
| Mouse Phenotypes | increased neuron apoptosis |
astrocytosis |
|
| Availability | Mouse Genotype | ||
| Hax1tm1Jni/Hax1tm1Jni | |||
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