Gene: EIF2B5 ×
Source: UNIPROT ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8893
Gene Symbol: EIF2B5
EIF2B5 		0.990 GeneticVariation disease UNIPROT Adult-onset leukoencephalopathies with vanishing white matter with novel missense mutations in EIF2B2, EIF2B3, and EIF2B5. 21484434 2011
Entrez Id: 8893
Gene Symbol: EIF2B5
EIF2B5 		0.990 GeneticVariation disease UNIPROT Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease. 19158808 2009
Entrez Id: 8893
Gene Symbol: EIF2B5
EIF2B5 		0.990 GeneticVariation disease UNIPROT Identification of ten novel mutations in patients with eIF2B-related disorders. 15776425 2005
Entrez Id: 8893
Gene Symbol: EIF2B5
EIF2B5 		0.990 GeneticVariation disease UNIPROT Ovarian failure related to eukaryotic initiation factor 2B mutations. 12707859 2003
Entrez Id: 8893
Gene Symbol: EIF2B5
EIF2B5 		0.990 GeneticVariation disease UNIPROT Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus. 12325082 2002
Entrez Id: 8893
Gene Symbol: EIF2B5
EIF2B5 		0.990 GeneticVariation disease UNIPROT Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter. 11704758 2001