Symbol Name ID |
Tgfb1
transforming growth factor, beta 1 MGI:98725 |
Darker colors indicate more annotations |
Human Phenotypes | Joint hemorrhage |
Mandibular prognathia |
Sinusitis |
Chronic sinusitis |
Sclerosis of skull base |
Genu valgum |
Cortical thickening of long bone diaphyses |
Diaphyseal sclerosis |
Clubbing of fingers |
Hip contracture |
Knee flexion contracture |
Abnormality of the elbow |
Joint swelling |
Bone pain |
Pathologic fracture |
Limb pain |
Lower limb pain |
Scoliosis |
Thoracolumbar scoliosis |
Vertebral compression fracture |
Increased bone mineral density |
Osteopenia |
Osteoporosis |
Arthritis |
Osteoarthritis |
Hyperostosis |
Narrowing of medullary canal |
Disease(s) Associated with TGFB1 | |||||||||||||||||||||||||||
Behcet's disease | |||||||||||||||||||||||||||
Camurati-Engelmann disease | |||||||||||||||||||||||||||
cystic fibrosis | |||||||||||||||||||||||||||
factor VIII deficiency | |||||||||||||||||||||||||||
multiple myeloma |
Mouse Phenotypes | abnormal tooth morphology |
abnormal incisor morphology |
abnormal incisor color |
misaligned incisors |
ameloblast degeneration |
abnormal tooth mineralization |
abnormal enamel morphology |
abnormal tooth attrition |
malocclusion |
kyphosis |
decreased osteoblast cell number |
abnormal bone ossification |
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Availability | Mouse Genotype | ||||||||||||
Tgfb1tm1(Tgfb3)Kul/Tgfb1tm1(Tgfb3)Kul |
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 07/05/2024 MGI 6.24 |
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