Symbol Name ID |
Tgfb2
transforming growth factor, beta 2 MGI:98726 |
Darker colors indicate more annotations |
Human Phenotypes | Flat cornea |
Ectopia lentis |
Deeply set eye |
Hypertelorism |
Ptosis |
Disease(s) Associated with TGFB2 | |||||
Loeys-Dietz syndrome 4 |
Mouse Phenotypes | abnormal iris stroma morphology |
absent Descemet membrane |
absent cornea endothelium |
decreased cornea thickness |
decreased cornea stroma thickness |
abnormal cornea stroma morphology |
abnormal cornea posterior stroma morphology |
fused cornea and lens |
absent eye anterior chamber |
abnormal eye posterior chamber morphology |
primary vitreous hyperplasia |
persistence of hyaloid vascular system |
abnormal retina neuronal layer morphology |
retina hyperplasia |
vitreous body deposition |
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Availability | Mouse Genotype | |||||||||||||||
Tgfb2tm1Doe/Tgfb2tm1Doe |
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 08/02/2024 MGI 6.24 |
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