Symbol Name ID |
Runx2
runt related transcription factor 2 MGI:99829 |
Darker colors indicate more annotations |
Human Phenotypes | Dystrophic fingernails |
Dystrophic toenail |
Disease(s) Associated with RUNX2 | ||
cleidocranial dysplasia |
Mouse Phenotypes | underdeveloped hair follicles |
abnormal skin morphology |
abnormal dermal layer morphology |
abnormal epidermis suprabasal layer morphology |
thin epidermis |
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Availability | Mouse Genotype | |||||
Runx2tm1Kish/Runx2tm1Kish | ||||||
Runx2tm1Mjo/Runx2+ |
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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