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Symbol Name ID |
Tgfb1
transforming growth factor, beta 1 MGI:98725 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Intracranial hemorrhage |
Intraventricular hemorrhage |
Dysphagia |
Optic nerve compression |
Easy fatigability |
Cranial nerve compression |
Spinal cord compression |
Depression |
Irritability |
Anxiety |
Waddling gait |
Headache |
Paresthesia |
| Disease(s) Associated with TGFB1 | |||||||||||||
| Behcet's disease | |||||||||||||
| Camurati-Engelmann disease | |||||||||||||
| cystic fibrosis | |||||||||||||
| eosinophilic esophagitis | |||||||||||||
| factor VIII deficiency | |||||||||||||
| multiple myeloma |
| Mouse Phenotypes | nervous system phenotype |
open neural tube |
brain inflammation |
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| Availability | Mouse Genotype | |||
| Tgfb1tm1Doe/Tgfb1tm1Doe | * | |||
| Tgfb1tm1N/Tgfb1tm1N | ||||
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 05/07/2024 MGI 6.23 |
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