Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C3280282
Disease: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT 		0.700 CausalMutation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C4693325
Disease: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE 		0.600 GeneticVariation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.110 GeneticVariation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		0.100 GeneticVariation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		0.100 CausalMutation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		0.100 GeneticVariation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		0.100 GeneticVariation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C2243051
Disease: Large head (disorder)
Large head (disorder) 		0.100 GeneticVariation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C4693964
Disease: NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE
NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS WITHOUT SEIZURES, AUTOSOMAL RECESSIVE 		0.100 CausalMutation CLINVAR

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.130 GeneticVariation CLINVAR Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus. 6306230

1983
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation CLINVAR Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus. 6306230

1983
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus. 6306230

1983
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 CausalMutation CLINVAR Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus. 6306230

1983
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.130 GeneticVariation CLINVAR Luteinizing hormone and follicle stimulating hormone secretion patterns in boys throughout puberty measured using highly sensitive immunoradiometric assays. 2516786

1989
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation CLINVAR Luteinizing hormone and follicle stimulating hormone secretion patterns in boys throughout puberty measured using highly sensitive immunoradiometric assays. 2516786

1989
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Luteinizing hormone and follicle stimulating hormone secretion patterns in boys throughout puberty measured using highly sensitive immunoradiometric assays. 2516786

1989
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 CausalMutation CLINVAR Luteinizing hormone and follicle stimulating hormone secretion patterns in boys throughout puberty measured using highly sensitive immunoradiometric assays. 2516786

1989
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.130 GeneticVariation CLINVAR Molecular cloning and characterization of the rat NMDA receptor. 1834949

1991
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation CLINVAR Molecular cloning and characterization of the rat NMDA receptor. 1834949

1991
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Molecular cloning and characterization of the rat NMDA receptor. 1834949

1991
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 CausalMutation CLINVAR Molecular cloning and characterization of the rat NMDA receptor. 1834949

1991
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.130 GeneticVariation CLINVAR Molecular cloning and chromosomal localization of the key subunit of the human N-methyl-D-aspartate receptor. 7679115

1993
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation CLINVAR Molecular cloning and chromosomal localization of the key subunit of the human N-methyl-D-aspartate receptor. 7679115

1993
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR Molecular cloning and chromosomal localization of the key subunit of the human N-methyl-D-aspartate receptor. 7679115

1993
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 CausalMutation CLINVAR Molecular cloning and chromosomal localization of the key subunit of the human N-methyl-D-aspartate receptor. 7679115

1993