Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Bilateral frontoparietal polymicrogyria: a novel GPR56 mutation and an unusual phenotype. 25642806

2015
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR The adhesion G protein-coupled receptor GPR56 is a cell-autonomous regulator of oligodendrocyte development. 25607655

2015
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR The adhesion G protein-coupled receptor GPR56 is a cell-autonomous regulator of oligodendrocyte development. 25607655

2015
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Bilateral frontoparietal polymicrogyria: a novel GPR56 mutation and an unusual phenotype. 25642806

2015
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning. 24531968

2014
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Compound heterozygosity in GPR56 with bilateral frontoparietal polymicrogyria. 23981349

2014
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning. 24531968

2014
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Compound heterozygosity in GPR56 with bilateral frontoparietal polymicrogyria. 23981349

2014
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR The N terminus of the adhesion G protein-coupled receptor GPR56 controls receptor signaling activity. 21708946

2011
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Disease-associated GPR56 mutations cause bilateral frontoparietal polymicrogyria via multiple mechanisms. 21349848

2011
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Disease-associated GPR56 mutations cause bilateral frontoparietal polymicrogyria via multiple mechanisms. 21349848

2011
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR The N terminus of the adhesion G protein-coupled receptor GPR56 controls receptor signaling activity. 21708946

2011
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. 20929962

2010
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. 20929962

2010
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations. 19016831

2009
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations. 19016831

2009
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes. 16240336

2005
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes. 16240336

2005
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. 12730993

2003
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation CLINVAR Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. 12730993

2003