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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Grm1 and autosomal recessive spinocerebellar ataxia 13 in Rattus norvegicus.        

  • 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 GRM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive spinocerebellar ataxia 13  (DOID:0080062)
  • 30 papers in RGD have been used to annotate Grm1


    • An association has been curated linking Grm1 and autosomal recessive spinocerebellar ataxia 13 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 GRM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive spinocerebellar ataxia 13  (DOID:0080062)
  • 30 papers in RGD have been used to annotate Grm1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive spinocerebellar ataxia 13 | ClinVar Annotator: match by term: GRM1-related condition
  • Original References(s): PMID:19146831 PMID:19924463 PMID:22448230 PMID:22558107 PMID:25741868 PMID:25741889 PMID:26308914 PMID:26467025 PMID:28492532 PMID:31319223


    • An association has been curated linking Grm1 and autosomal recessive spinocerebellar ataxia 13 in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Grm1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive spinocerebellar ataxia 13  (DOID:0080062)
  • 30 papers in RGD have been used to annotate Grm1
  • Curation Notes: OMIM:614831


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