Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C4015505
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 		0.900 GeneticVariation UNIPROT Structural basis for integration of GluD receptors within synaptic organizer complexes. 27418511

2016
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C4015505
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 		0.900 GeneticVariation UNIPROT GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia. 25841024

2015
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C4015505
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 		0.900 GeneticVariation UNIPROT A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy. 23611888

2013
Entrez Id: 2895
Gene Symbol: GRID2
GRID2
CUI: C4015505
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 		0.900 GeneticVariation UNIPROT Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans. 24078737

2013