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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

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

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with GRIN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 0 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 Canis lupus familiaris.        

  • 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 GRIN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with or without Hyperkinetic Movements and Seizures, Autosomal Recessive  (DOID:9009115)
  • 0 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:22833210 PMID:25741868 PMID:26350515 PMID:26467025 PMID:27159321 PMID:27164704 PMID:28051072 PMID:28492532 PMID:30776697


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