Symbol Name ID |
Runx2
runt related transcription factor 2 MGI:99829 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Short stature |
Moderately short stature |
Severe short stature |
Disease(s) Associated with RUNX2 | |||
cleidocranial dysplasia | |||
metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome |
Mouse Phenotypes | abnormal incisor morphology |
small incisors |
abnormal molar morphology |
small molars |
abnormal tooth development |
abnormal dental lamina morphology |
abnormal dental papilla morphology |
abnormal cervical loop morphology |
abnormal enamel knot morphology |
arrest of tooth development |
growth retardation of incisors |
growth retardation of molars |
abnormal dentin morphology |
abnormal enamel morphology |
abnormal nasal bone morphology |
nasal bone hypoplasia |
palatal shelves fail to meet at midline |
cleft secondary palate |
abnormal nose morphology |
growth/size/body region phenotype |
decreased birth weight |
decreased birth body size |
increased lean body mass |
decreased body weight |
slow postnatal weight gain |
decreased body size |
disproportionate dwarf |
enlarged spleen |
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Availability | Mouse Genotype | ||||||||||||||||||||||||||||
Runx2tm1Kish/Runx2tm1Kish | |||||||||||||||||||||||||||||
Runx2tm1Ldq/Runx2tm1Ldq | |||||||||||||||||||||||||||||
Runx2tm1Mjo/Runx2tm1Mjo | |||||||||||||||||||||||||||||
Runx2em1(IMPC)Rbrc/Runx2+ | |||||||||||||||||||||||||||||
Runx2tm1Gss/Runx2+ | |||||||||||||||||||||||||||||
Runx2tm1Kish/Runx2+ | * | ||||||||||||||||||||||||||||
Runx2tm1Ldq/Runx2+ | |||||||||||||||||||||||||||||
Runx2tm1Mjo/Runx2+ | |||||||||||||||||||||||||||||
Runx2tm1Javed/Runx2tm1Javed Tg(Col2a1-cre)1Bhr/0 (conditional) |
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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