Gene: FAS ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR Differential regulation of miR-146a/FAS and miR-21/FASLG axes in autoimmune lymphoproliferative syndrome due to FAS mutation (ALPS-FAS). 27060458 2016
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations. 24398331 2014
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR Autoimmune lymphoproliferative syndrome: an update and review of the literature. 25086580 2014
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation. 21885602 2011
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndrome. 21490157 2011
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR Somatic FAS mutations are common in patients with genetically undefined autoimmune lymphoproliferative syndrome. 20360470 2010
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR Autoimmune lymphoproliferative syndrome (ALPS) in a child from consanguineous parents: a dominant or recessive disease? 10709732 2000
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR Missense mutations in the Fas gene resulting in autoimmune lymphoproliferative syndrome: a molecular and immunological analysis. 9028321 1997
Entrez Id: 355
Gene Symbol: FAS
FAS 		0.100 CausalMutation phenotype CLINVAR Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity. 7539157 1995