GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Pnpla6 and hereditary spastic paraplegia 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 PNPLA6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 121 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 6 papers in RGD have been used to annotate Pnpla6
  • Curation Notes: ClinVar Annotator: match by term: Spastic Paraplegia, Recessive
  • Original References(s): PMID:26467025, PMID:28492532

  • This annotation was curated on 2019-05-14 05:28:04.0 by RGD . For more information contact us

    An association has been curated linking Pnpla6 and hereditary spastic paraplegia 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 PNPLA6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 121 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 6 papers in RGD have been used to annotate Pnpla6
  • Curation Notes: ClinVar Annotator: match by term: Spastic Paraplegia, Recessive

  • This annotation was curated on 2019-05-14 05:27:53.0 by RGD . For more information contact us

    An association has been curated linking Pnpla6 and hereditary spastic paraplegia 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 PNPLA6 (Homo sapiens) [(EXP) inferred from experiment]
  • 121 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 6 papers in RGD have been used to annotate Pnpla6
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:20382209

  • This annotation was curated on 2019-05-14 04:41:58.0 by RGD . For more information contact us

    An association has been curated linking Pnpla6 and hereditary spastic paraplegia 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 PNPLA6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 121 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 6 papers in RGD have been used to annotate Pnpla6
  • Curation Notes: ClinVar Annotator: match by term: Spastic Paraplegia, Recessive
  • Original References(s): PMID:28492532

  • This annotation was curated on 2019-05-14 05:28:06.0 by RGD . For more information contact us

    An association has been curated linking Pnpla6 and hereditary spastic paraplegia 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 PNPLA6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 121 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 6 papers in RGD have been used to annotate Pnpla6
  • Curation Notes: ClinVar Annotator: match by term: Spastic Paraplegia, Recessive
  • Original References(s): PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2019-05-14 05:28:08.0 by RGD . For more information contact us

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