Gene: RANBP2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5903
Gene Symbol: RANBP2
RANBP2 		0.050 GeneticVariation disease BEFREE Familial acute necrotizing encephalopathy with RANBP2 mutation: The first report in Northeast Asia. 28336122 2017
Entrez Id: 5903
Gene Symbol: RANBP2
RANBP2 		0.050 GeneticVariation disease BEFREE RANBP2 mutation in an Indian child with recurrent acute necrotizing encephalopathy. 27591117 2016
Entrez Id: 5903
Gene Symbol: RANBP2
RANBP2 		0.050 GeneticVariation disease BEFREE We believe that this is the first description implicating the H1N1 viral strain as a trigger and the second report of a T653I mutation in the RANBP2 gene described in relation to ANE1. 25170550 2015
Entrez Id: 5903
Gene Symbol: RANBP2
RANBP2 		0.050 GeneticVariation disease BEFREE Familial acute necrotizing encephalopathy due to mutation in the RANBP2 gene. 25128471 2014
Entrez Id: 5903
Gene Symbol: RANBP2
RANBP2 		0.050 GeneticVariation disease BEFREE Untreated recurrent acute necrotising encephalopathy associated with RANBP2 mutation, and normal outcome in a Caucasian boy. 20473521 2010