Gene: GCGR ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2642
Gene Symbol: GCGR
GCGR 		0.020 GeneticVariation disease BEFREE Glucagon receptor (GCGR) defect (Mahvash disease) is an autosomal recessive hereditary pancreatic neuroendocrine tumor (PNET) syndrome that has only been reported in adults with pancreatic α cell hyperplasia and PNETs. 30294546 2018
Entrez Id: 2642
Gene Symbol: GCGR
GCGR 		0.020 GeneticVariation disease BEFREE Homozygous P86S mutation of the human glucagon receptor is associated with hyperglucagonemia, alpha cell hyperplasia, and islet cell tumor. 19657311 2009