Symbol Name ID |
Runx2
runt related transcription factor 2 MGI:99829 |
Darker colors indicate more annotations |
Human Phenotypes | Sinusitis |
Chronic otitis media |
Recurrent respiratory infections |
Disease(s) Associated with RUNX2 | |||
cleidocranial dysplasia |
Mouse Phenotypes | abnormal osteoclast differentiation |
enlarged thymus |
decreased thymocyte number |
enlarged spleen |
increased granulocyte number |
decreased B cell number |
increased osteoclast cell number |
abnormal splenic cell ratio |
|
Availability | Mouse Genotype | ||||||||
Runx2tm1Kish/Runx2tm1Kish | |||||||||
Runx2tm1Kish/Runx2+ | |||||||||
Tg(Col1a1-Runx2)#Pmt/0 |
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 05/14/2024 MGI 6.23 |
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