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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking Hint1 and Gamstorp-Wohlfart syndrome 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by OMIM:137200
  • Original References(s): PMID:22961002


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by OMIM:137200
  • Original References(s): PMID:1851512, PMID:22961002


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by term: Neuromyotonia and axonal neuropathy, autosomal recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive axonal neuropathy with neuromyotonia
  • Original References(s): PMID:31400136


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive axonal neuropathy with neuromyotonia
  • Original References(s): PMID:22961002, PMID:25342199, PMID:28492532, PMID:29787766


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by term: Neuromyotonia and axonal neuropathy, autosomal recessive
  • Original References(s): PMID:22961002, PMID:25342199, PMID:26182879, PMID:27549087, PMID:28492532


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by term: Neuromyotonia and axonal neuropathy, autosomal recessive
  • Original References(s): PMID:25741868


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by term: Neuromyotonia and axonal neuropathy, autosomal recessive
  • Original References(s): PMID:22961002, PMID:28492532


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive axonal neuropathy with neuromyotonia


  • An association has been curated linking Hint1 and Gamstorp-Wohlfart 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 HINT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Gamstorp-Wohlfart syndrome  (DOID:0050526)
  • 4 papers in RGD have been used to annotate Hint1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive axonal neuropathy with neuromyotonia
  • Original References(s): PMID:22961002, PMID:25342199, PMID:26182879, PMID:27549087, PMID:28492532, PMID:30311386


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.