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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking GRIN1 and Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11051505 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 22 papers in RGD have been used to annotate GRIN1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25741868 PMID:26350515 PMID:27164704 PMID:28051072


    • An association has been curated linking GRIN1 and Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 22 papers in RGD have been used to annotate GRIN1


    • An association has been curated linking GRIN1 and Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13531759 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 22 papers in RGD have been used to annotate GRIN1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:25741868 PMID:27159321 PMID:27164704 PMID:28492532 PMID:30776697


    • An association has been curated linking GRIN1 and Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13622384 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 22 papers in RGD have been used to annotate GRIN1
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive
  • Original References(s): PMID:22833210 PMID:25741868 PMID:28492532


    • An association has been curated linking GRIN1 and Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8659670|RGD:8659673 (Homo sapiens) & RGD:8659670|RGD:8659673 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 22 papers in RGD have been used to annotate GRIN1
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking GRIN1 and Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13485668|RGD:150436071|RGD:38461712|RGD:38462812|RGD:38463731|RGD:405004830 (Homo sapiens) & RGD:13485668|RGD:150436071|RGD:38461712|RGD:38462812|RGD:38463731|RGD:405004830 (Homo sapiens) & RGD:13485668|RGD:150436071|RGD:38461712|RGD:38462812|RGD:38463731|RGD:405004830 (Homo sapiens) & RGD:13485668|RGD:150436071|RGD:38461712|RGD:38462812|RGD:38463731|RGD:405004830 (Homo sapiens) & RGD:13485668|RGD:150436071|RGD:38461712|RGD:38462812|RGD:38463731|RGD:405004830 (Homo sapiens) & RGD:13485668|RGD:150436071|RGD:38461712|RGD:38462812|RGD:38463731|RGD:405004830 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 22 papers in RGD have been used to annotate GRIN1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE | ClinVar Annotator: match by term: Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive
  • Original References(s): PMID:25741868


    • An association has been curated linking GRIN1 and Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12833959|RGD:14398989|RGD:14398991|RGD:8659674 (Homo sapiens) & RGD:12833959|RGD:14398989|RGD:14398991|RGD:8659674 (Homo sapiens) & RGD:12833959|RGD:14398989|RGD:14398991|RGD:8659674 (Homo sapiens) & RGD:12833959|RGD:14398989|RGD:14398991|RGD:8659674 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 22 papers in RGD have been used to annotate GRIN1
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive
  • Original References(s): PMID:25741868 PMID:28492532


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