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Symbol
Name
ID
Runx2
runt related transcription factor 2
MGI:99829
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Frontal bossing
Parietal bossing
Brachycephaly
Thickened calvaria
Micrognathia
Mandibular prognathia
Hypoplasia of the maxilla
Absent frontal sinuses
Hypoplastic frontal sinuses
Absent paranasal sinuses
Sinusitis
Hypoplasia of the zygomatic bone
Malar flattening
Large foramen magnum
Decreased skull ossification
Macrocephaly
Persistent open anterior fontanelle
Wormian bones
Large fontanelles
Short face
Midface retrusion
Dimple chin
Broad forehead
Sloping forehead
Short philtrum
Thin vermilion border
Cleft palate
High palate
High, narrow palate
Narrow palate
Glossoptosis
Abnormality of the dentition
Supernumerary tooth
Delayed eruption of teeth
Delayed eruption of permanent teeth
Delayed eruption of primary teeth
Abnormal dental enamel morphology
Enamel hypoplasia
Carious teeth
Premature loss of teeth
Open bite
Convex nasal ridge
Depressed nasal bridge
Wide nasal bridge
Disease(s) Associated with RUNX2
cleidocranial dysplasia
metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome

Mouse Phenotypes
abnormal craniofacial bone morphology
abnormal cranial suture morphology
wide cranial sutures
abnormal cranium morphology
small basisphenoid bone
abnormal neurocranium morphology
abnormal fontanelle morphology
large anterior fontanelle
abnormal interparietal bone morphology
interparietal bone hypoplasia
abnormal supraoccipital bone morphology
absent occipital bone
abnormal parietal bone morphology
parietal bone hypoplasia
absent zygomatic arch
abnormal hyoid bone morphology
hyoid bone hypoplasia
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
abnormal zygomatic bone morphology
palatal shelves fail to meet at midline
cleft secondary palate
abnormal nose morphology
Availability Mouse Genotype
Runx2tm1Gss/Runx2tm1Gss
Runx2tm1Hkiy/Runx2tm1Hkiy
Runx2tm1Jals/Runx2tm1Jals
Runx2tm1Kish/Runx2tm1Kish
Runx2tm1Ldq/Runx2tm1Ldq
Runx2tm1Mjo/Runx2tm1Mjo
Runx2em1(IMPC)Rbrc/Runx2+
Runx2tm1Gss/Runx2+
Runx2tm1Kish/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
04/16/2024
MGI 6.23
The Jackson Laboratory