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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking Tdp1 and spinocerebellar ataxia type 1 with axonal neuropathy 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 TDP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 1 with axonal neuropathy  (DOID:0090115)
  • 6 papers in RGD have been used to annotate Tdp1


  • An association has been curated linking Tdp1 and spinocerebellar ataxia type 1 with axonal neuropathy 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 TDP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 1 with axonal neuropathy  (DOID:0090115)
  • 6 papers in RGD have been used to annotate Tdp1
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
  • Original References(s): PMID:26467025


  • An association has been curated linking Tdp1 and spinocerebellar ataxia type 1 with axonal neuropathy 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 TDP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 1 with axonal neuropathy  (DOID:0090115)
  • 6 papers in RGD have been used to annotate Tdp1
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1


  • An association has been curated linking Tdp1 and spinocerebellar ataxia type 1 with axonal neuropathy 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 TDP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 1 with axonal neuropathy  (DOID:0090115)
  • 6 papers in RGD have been used to annotate Tdp1
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
  • Original References(s): PMID:12244316


  • An association has been curated linking Tdp1 and spinocerebellar ataxia type 1 with axonal neuropathy 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 TDP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 1 with axonal neuropathy  (DOID:0090115)
  • 6 papers in RGD have been used to annotate Tdp1
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Tdp1 and spinocerebellar ataxia type 1 with axonal neuropathy 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 TDP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 1 with axonal neuropathy  (DOID:0090115)
  • 6 papers in RGD have been used to annotate Tdp1
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
  • Original References(s): PMID:25741868 PMID:26467025


  • An association has been curated linking Tdp1 and spinocerebellar ataxia type 1 with axonal neuropathy 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 TDP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 1 with axonal neuropathy  (DOID:0090115)
  • 6 papers in RGD have been used to annotate Tdp1
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
  • Original References(s): PMID:24355542 PMID:26467025


  • An association has been curated linking Tdp1 and spinocerebellar ataxia type 1 with axonal neuropathy 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 TDP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to spinocerebellar ataxia type 1 with axonal neuropathy  (DOID:0090115)
  • 6 papers in RGD have been used to annotate Tdp1
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1
  • Original References(s): PMID:28492532


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