Gene: TNFSF11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 Biomarker disease MGD Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology. 26234751 2016
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 Biomarker disease MGD A RANKL G278R mutation causing osteopetrosis identifies a functional amino acid essential for trimer assembly in RANKL and TNF. 22068587 2012
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 Biomarker disease MGD Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO. 22836362 2012
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 Biomarker disease MGD Epidermal receptor activator of NF-kappaB ligand controls Langerhans cells numbers and proliferation. 18606662 2008
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 GeneticVariation disease UNIPROT Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL. 17632511 2007
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 Biomarker disease MGD Regulation of peripheral lymph node genesis by the tumor necrosis factor family member TRANCE. 11085748 2000
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 Biomarker disease MGD Diverse roles of the tumor necrosis factor family member TRANCE in skeletal physiology revealed by TRANCE deficiency and partial rescue by a lymphocyte-expressed TRANCE transgene. 10984520 2000
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 Biomarker disease CTD_human
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11 		0.800 Biomarker disease GENOMICS_ENGLAND