Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10020
Gene Symbol: GNE
GNE 		0.540 GeneticVariation disease BEFREE Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy. 15833430 2005
Entrez Id: 10020
Gene Symbol: GNE
GNE 		0.540 GeneticVariation disease BEFREE Novel missense mutation and large deletion of GNE gene in autosomal-recessive inclusion-body myopathy. 12811782 2003
Entrez Id: 10020
Gene Symbol: GNE
GNE 		0.540 GeneticVariation disease BEFREE GNE mutations are known to cause two other disorders: sialuria (OMIM #269921) and autosomal recessive inclusion body myopathy (IBM2, OMIM #600737). 11916006 2002
Entrez Id: 10020
Gene Symbol: GNE
GNE 		0.540 Biomarker disease CTD_human An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE gene. 12473780 2002
Entrez Id: 10020
Gene Symbol: GNE
GNE 		0.540 GeneticVariation disease BEFREE Analysis for GNE mutations was performed in an American, non-Iranian Jewish, family with quadriceps-sparing inclusion body myopathy (QS-IBM) and in 11 patients with sporadic IBM (s-IBM). 12473769 2002
Entrez Id: 10020
Gene Symbol: GNE
GNE 		0.540 GermlineCausalMutation disease ORPHANET Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE). 11916006 2002