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Symbol
Name
ID

Runx2
runt related transcription factor 2
MGI:99829

Phenotype annotations related to respiratory system

Darker colors indicate more annotations

Human Phenotypes	Absent frontal sinuses	Hypoplastic frontal sinuses	Absent paranasal sinuses	Sinusitis	Recurrent respiratory infections	Respiratory distress	Neonatal respiratory distress
Disease(s) Associated with RUNX2
cleidocranial dysplasia

Mouse Phenotypes		pulmonary vascular congestion	abnormal nasal bone morphology	nasal bone hypoplasia	abnormal nose morphology	abnormal lung volume	respiratory distress	respiratory failure
Availability	Mouse Genotype	pulmonary vascular congestion	abnormal nasal bone morphology	nasal bone hypoplasia	abnormal nose morphology	abnormal lung volume	respiratory distress	respiratory failure
	Runx2^tm1Kish/Runx2^tm1Kish
	Runx2^tm1Ldq/Runx2^tm1Ldq
	Runx2^tm1Mjo/Runx2^tm1Mjo
	Runx2^tm1Kish/Runx2⁺
	Runx2^tm1.1Yyon/Runx2^tm1.1Yyon Tg(Col2a1-cre)1Star/0 (conditional)
	Runx2^tm1Javed/Runx2^tm1Javed 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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