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Symbol Name ID |
Runx2
runt related transcription factor 2 MGI:99829 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypertelorism |
| Disease(s) Associated with RUNX2 | |
| cleidocranial dysplasia |
| Mouse Phenotypes | eyelids open at birth |
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| Availability | Mouse Genotype | |
| Runx2tm1Mjo/Runx2tm1Mjo | ||
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 04/30/2024 MGI 6.23 |
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