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Symbol
Name
ID
Runx2
runt related transcription factor 2
MGI:99829
Phenotype annotations related to growth/size/body
*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
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)

Contributing Projects:
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
The Jackson Laboratory