Symbol Name ID |
Tgfbr2
transforming growth factor, beta receptor II MGI:98729 |
Darker colors indicate more annotations |
Human Phenotypes | Pulmonary artery dilatation |
Pulmonary artery aneurysm |
Pneumothorax |
Spontaneous pneumothorax |
Emphysema |
Laryngeal carcinoma |
Disease(s) Associated with TGFBR2 | ||||||
Loeys-Dietz syndrome 2 | ||||||
Lynch syndrome | ||||||
Marfan syndrome |
Mouse Phenotypes | hemothorax |
abnormal nasal septum morphology |
abnormal branching involved in lung morphogenesis |
abnormal lung lobe morphology |
abnormal bronchus morphology |
abnormal bronchial cartilage morphology |
dilated respiratory conducting tube |
abnormal tracheal cartilage morphology |
decreased tracheal cartilage ring number |
respiratory distress |
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Availability | Mouse Genotype | ||||||||||
Tgfbr2tm1.1Hcd/Tgfbr2+ | |||||||||||
Tg(CD2-Tgfbr2)1Grs/? | |||||||||||
Tgfbr2tm1.2Hlm/Tgfbr2tm1.2Hlm Twist2tm1(cre)Dor/Twist2+ (conditional) |
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Tgfbr2tm1.2Hlm/Tgfbr2tm1.2Hlm Tg(KRT14-cre)52Smr/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 05/14/2024 MGI 6.23 |
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