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 |
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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) |
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last database update 09/03/2024 MGI 6.24 |
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