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GENE - TERM ANNOTATION REPORT

21 Annotations Found.

An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:20037588


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:22851605 PMID:25741868 PMID:26467025 PMID:28492532 PMID:28898540


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:20037586 PMID:20037587 PMID:20037588 PMID:20104247 PMID:20460441 PMID:21288981 PMID:21336783 PMID:21454511 PMID:22702953 PMID:24575025 PMID:24789864 PMID:25256292 PMID:25741868 PMID:25900305 PMID:26110311 PMID:26467025 PMID:28492532 PMID:4056805 PMID:8179305


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:20037586 PMID:20037587 PMID:20037588 PMID:20460441 PMID:21336783 PMID:22702953 PMID:24575025 PMID:24789864 PMID:24963089 PMID:25900305 PMID:26110311 PMID:26467025 PMID:26948711 PMID:27751652 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:20037586 PMID:22675077 PMID:24789864 PMID:26467025 PMID:27549087 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:22851605 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:19666518 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII
  • Original References(s): PMID:25741868


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII
  • Original References(s): PMID:25741868 PMID:25900305 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:26392352 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:15668982 PMID:20037588 PMID:20460441 PMID:21115951 PMID:21454511 PMID:22065612 PMID:22702953 PMID:25741868 PMID:26467025 PMID:28492532 PMID:8179305


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:22419508 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:22689196 PMID:22851605 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:19661060 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Trpv4 and distal hereditary motor neuronopathy type 8 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 TRPV4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to distal hereditary motor neuronopathy type 8  (DOID:0111215)
  • 12 papers in RGD have been used to annotate Trpv4
  • Curation Notes: ClinVar Annotator: match by term: Distal spinal muscular atrophy, congenital nonprogressive
  • Original References(s): PMID:10463355 PMID:20460441 PMID:21288981 PMID:22291064 PMID:22526352 PMID:22702953 PMID:24789864 PMID:25741868 PMID:26048687 PMID:26467025 PMID:26948711 PMID:28492532


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