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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with GRIN2A (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:23933820


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:26283219 PMID:26467025 PMID:27839871 PMID:28492532


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:26220384 PMID:28492532


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:28492532


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: Acquired epileptiform aphasia
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:25741868


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:23933819 PMID:25741868 PMID:26220384 PMID:26467025 PMID:28492532 PMID:29124671


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:18414213 PMID:23933819 PMID:25726841 PMID:25904555 PMID:26467025 PMID:26601054 PMID:27288002 PMID:28492532 PMID:29358611


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:23933819 PMID:23933820 PMID:25164438 PMID:25741868 PMID:26467025 PMID:27640074 PMID:28492532 PMID:29124671


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:23408766 PMID:23933818 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:27171548 PMID:28492532


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: APHASIA, ACQUIRED, WITH EPILEPSY
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26220384 PMID:28492532 PMID:29124671


  • An association has been curated linking Grin2a and Landau-Kleffner syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with GRIN2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Landau-Kleffner syndrome  (DOID:2538)
  • 104 papers in RGD have been used to annotate Grin2a
  • Curation Notes: ClinVar Annotator: match by term: Acquired epileptiform aphasia
  • Original References(s): PMID:20890276 PMID:21559497 PMID:25741868 PMID:25904555 PMID:26467025 PMID:28492532


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