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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking CYP2U1 and hereditary spastic paraplegia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13817016 (Homo sapiens)
  • 632 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 7 papers in RGD have been used to annotate CYP2U1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532 PMID:36166872


    • An association has been curated linking CYP2U1 and hereditary spastic paraplegia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:127257406 (Homo sapiens)
  • 632 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 7 papers in RGD have been used to annotate CYP2U1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29034544


    • An association has been curated linking CYP2U1 and hereditary spastic paraplegia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8570472 (Homo sapiens)
  • 632 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 7 papers in RGD have been used to annotate CYP2U1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:14660610 PMID:23176821 PMID:25741868 PMID:28492532 PMID:29034544 PMID:33107650


    • An association has been curated linking CYP2U1 and hereditary spastic paraplegia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens) & RGD:150483664|RGD:150499621|RGD:151754656|RGD:151754663|RGD:151754674|RGD:151754681|RGD:151754686|RGD:151754703|RGD:151754710|RGD:151754720|RGD:151754726|RGD:151754739|RGD:151754747 (Homo sapiens)
  • 632 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 7 papers in RGD have been used to annotate CYP2U1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


    • An association has been curated linking CYP2U1 and hereditary spastic paraplegia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens) & RGD:11349290|RGD:127287923|RGD:12886067|RGD:13467969|RGD:13488421|RGD:13540371|RGD:14709626|RGD:15119618|RGD:15121110|RGD:15121236|RGD:151754734|RGD:38460032|RGD:38467207 (Homo sapiens)
  • 632 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 7 papers in RGD have been used to annotate CYP2U1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


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