Homo sapiens Protein: TNFRSF11B | |||||||||||||||||||||||||
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Summary | |||||||||||||||||||||||||
InnateDB Protein | IDBP-33677.6 | ||||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||||
Gene Symbol | TNFRSF11B | ||||||||||||||||||||||||
Protein Name | tumor necrosis factor receptor superfamily, member 11b | ||||||||||||||||||||||||
Synonyms | OCIF; OPG; TR1; | ||||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||||
Ensembl Protein | ENSP00000297350 | ||||||||||||||||||||||||
InnateDB Gene | IDBG-33675 (TNFRSF11B) | ||||||||||||||||||||||||
Protein Structure | |||||||||||||||||||||||||
UniProt Annotation | |||||||||||||||||||||||||
Function | Acts as decoy receptor for TNFSF11/RANKL and thereby neutralizes its function in osteoclastogenesis. Inhibits the activation of osteoclasts and promotes osteoclast apoptosis in vitro. Bone homeostasis seems to depend on the local ratio between TNFSF11 and TNFRSF11B. May also play a role in preventing arterial calcification. May act as decoy receptor for TNFSF10/TRAIL and protect against apoptosis. TNFSF10/TRAIL binding blocks the inhibition of osteoclastogenesis. {ECO:0000269PubMed:22664871, ECO:0000269PubMed:9168977}. | ||||||||||||||||||||||||
Subcellular Localization | Secreted. | ||||||||||||||||||||||||
Disease Associations | Juvenile Paget disease (JPD) [MIM:239000]: Rare autosomal recessive osteopathy that presents in infancy or early childhood. The disorder is characterized by rapidly remodeling woven bone, osteopenia, debilitating fractures, and deformities due to a markedly accelerated rate of bone remodeling throughout the skeleton. Approximately 40 cases of JPD have been reported worldwide. Unless it is treated with drugs that block osteoclast- mediated skeletal resorption, the disease can be fatal. {ECO:0000269PubMed:12189164}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||||
Tissue Specificity | Highly expressed in adult lung, heart, kidney, liver, spleen, thymus, prostate, ovary, small intestine, thyroid, lymph node, trachea, adrenal gland, testis, and bone marrow. Detected at very low levels in brain, placenta and skeletal muscle. Highly expressed in fetal kidney, liver and lung. | ||||||||||||||||||||||||
Comments | |||||||||||||||||||||||||
Interactions | |||||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||||
InterPro |
IPR000488
Death domain IPR001368 TNFR/NGFR cysteine-rich region IPR011029 Death-like domain IPR017371 Tumour necrosis factor receptor 11B IPR022323 Tumour necrosis factor receptor 11 |
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PFAM |
PF00531
PF00020 |
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PRINTS |
PR01975
PR01961 |
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PIRSF |
PIRSF038065
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SMART |
SM00005
SM00208 |
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TIGRFAMs | |||||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||||
Modification | |||||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||||
SwissProt | O00300 | ||||||||||||||||||||||||
PhosphoSite | PhosphoSite-O00300 | ||||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||||
Entrez Gene | 4982 | ||||||||||||||||||||||||
UniGene | Hs.81791 | ||||||||||||||||||||||||
RefSeq | NP_002537 | ||||||||||||||||||||||||
HUGO | HGNC:11909 | ||||||||||||||||||||||||
OMIM | 602643 | ||||||||||||||||||||||||
CCDS | CCDS6326 | ||||||||||||||||||||||||
HPRD | 04032 | ||||||||||||||||||||||||
IMGT | |||||||||||||||||||||||||
EMBL | AB002146 AB008822 AC107953 AF134187 AK223155 AK313710 AP004283 AY466112 BC030155 U94332 | ||||||||||||||||||||||||
GenPept | AAB53709 AAF20168 AAH30155 AAR23265 BAA25910 BAA32076 BAD96875 BAG36455 | ||||||||||||||||||||||||