Symbol Name ID |
Tnfsf11
tumor necrosis factor (ligand) superfamily, member 11 MGI:1100089 |
Darker colors indicate more annotations |
Human Phenotypes | Cranial hyperostosis |
Mandibular osteomyelitis |
Mandibular prognathia |
Facial paralysis |
Persistence of primary teeth |
Carious teeth |
Chronic rhinitis due to narrow nasal airway |
Disease(s) Associated with TNFSF11 | |||||||
autosomal recessive osteopetrosis 2 |
Mouse Phenotypes | abnormal craniofacial bone morphology |
abnormal cranial suture morphology |
optic canal stenosis |
decreased cranium height |
small cranium |
abnormal neurocranium morphology |
thin neurocranium |
abnormal hyoid bone body morphology |
failure of tooth eruption |
supernumerary teeth |
mandible hypoplasia |
abnormal zygomatic bone morphology |
round face |
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Availability | Mouse Genotype | |||||||||||||
Tnfsf11gum/Tnfsf11gum | ||||||||||||||
Tnfsf11tles/Tnfsf11tles | ||||||||||||||
Tnfsf11tm1.2Htaka/Tnfsf11tm1.2Htaka | ||||||||||||||
Tnfsf11tm1Pngr/Tnfsf11tm1Pngr | ||||||||||||||
Tnfsf11tm1Ywc/Tnfsf11tm1Ywc | ||||||||||||||
Tnfsf11tles/Tnfsf11tm1Pngr | ||||||||||||||
Tnfsf11tm1.1Caob/Tnfsf11tm1.1Caob Tg(BGLAP-cre)1Clem/0 (conditional) |
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Tnfsf11tm1.1Caob/Tnfsf11tm1.1Caob Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/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 04/16/2024 MGI 6.23 |
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