Symbol Name ID |
Tnfrsf11b
tumor necrosis factor receptor superfamily, member 11b (osteoprotegerin) MGI:109587 |
Darker colors indicate more annotations |
Human Phenotypes | Cranial hyperostosis |
Thickened calvaria |
Macrocephaly |
Relative macrocephaly |
Abnormality of the dentition |
Premature loss of teeth |
Disease(s) Associated with TNFRSF11B | ||||||
Paget's disease of bone 5 |
Mouse Phenotypes | otosclerosis |
abnormal parietal bone morphology |
thin parietal bone |
abnormal mandible morphology |
abnormal middle ear ossicle morphology |
abnormal incus body morphology |
abnormal malleus morphology |
abnormal stapes morphology |
abnormal stapes annular ligament morphology |
abnormal stapes footplate morphology |
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Availability | Mouse Genotype | ||||||||||
Tnfrsf11btm1Eac/Tnfrsf11btm1Eac | |||||||||||
Tnfrsf11btm1Khs/Tnfrsf11btm1Khs | |||||||||||
Tnfrsf11btm1Wss/Tnfrsf11btm1Wss |
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 04/16/2024 MGI 6.23 |
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