{"symbol":"IFNGR2","synonyms":["IMD28","AF-1","IFGR2","IFNGT1"],"name":"interferon gamma receptor 2 (interferon gamma transducer 1)","description":"This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":3460,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/3460","proteins":[{"symbol":"INGR2_HUMAN","href":"/api/1.0/protein/INGR2_HUMAN"}],"hgncRootFamilies":[{"name":"Interferon receptors","href":"/api/1.0/gene_family/Interferon+receptors"},{"name":"Fibronectin type III domain containing","href":"/api/1.0/gene_family/Fibronectin+type+III+domain+containing"}]}