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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking SPG7 and genetic disease 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:12895710 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:11222789 PMID:18799786 PMID:21623769 PMID:22554690 PMID:22571692 PMID:22964162 PMID:23065789 PMID:23269439 PMID:23812641 PMID:24033266 PMID:24466038 PMID:24727571 PMID:24731568 PMID:25741868 PMID:26094131 PMID:26260707 PMID:26374131 PMID:26467025 PMID:26626314 PMID:26671083 PMID:26756429 PMID:27084228 PMID:27165006 PMID:27217339 PMID:27260292 PMID:28492532 PMID:28608987 PMID:28832565 PMID:29026558 PMID:29915382 PMID:30533525 PMID:31068484 PMID:31345272 PMID:31433872 PMID:31692161 PMID:32161564


    • An association has been curated linking SPG7 and genetic disease 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:14718094 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SPG7 and genetic disease 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:8597269 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:11478530 PMID:15507752 PMID:17384005 PMID:18414213 PMID:18799786 PMID:19841671 PMID:20186691 PMID:21623769 PMID:22964162 PMID:23065789 PMID:23269439 PMID:23733235 PMID:23812641 PMID:23953397 PMID:24401005 PMID:25034272 PMID:25133958 PMID:25277871 PMID:25741868 PMID:25850353 PMID:26244503 PMID:26365338 PMID:26467025 PMID:26626314 PMID:27016405 PMID:2779008 PMID:27790088 PMID:28492532 PMID:29431110 PMID:30533525 PMID:30747022 PMID:31980526 PMID:32153640 PMID:32270516 PMID:32447552


    • An association has been curated linking SPG7 and genetic disease 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:14714885 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:22964162 PMID:25741868 PMID:28492532


    • An association has been curated linking SPG7 and genetic disease 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:151731148 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:30497413


    • An association has been curated linking SPG7 and genetic disease 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:10410050 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:16534102 PMID:25741868 PMID:26467025 PMID:28492532 PMID:32483926 PMID:33841295


    • An association has been curated linking SPG7 and genetic disease 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:8605002 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:11222789 PMID:14985266 PMID:16534102 PMID:17661097 PMID:18200586 PMID:18799786 PMID:20186691 PMID:21623769 PMID:22571692 PMID:22964162 PMID:23065789 PMID:23269439 PMID:23733235 PMID:24033266 PMID:24727571 PMID:25497598 PMID:25681447 PMID:25741868 PMID:26467025 PMID:26506339 PMID:26626314 PMID:27084228 PMID:27165006 PMID:27957547 PMID:28362824 PMID:28444220 PMID:28492532 PMID:28832565 PMID:29026558 PMID:29057857 PMID:29246844 PMID:29915382 PMID:30098094 PMID:30537300 PMID:32581362 PMID:32973427


    • An association has been curated linking SPG7 and genetic disease 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:10042293 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:21623769 PMID:22964162 PMID:24727571 PMID:25741868 PMID:26467025 PMID:26756429 PMID:27217339 PMID:28362824 PMID:28492532 PMID:28812649 PMID:29057857 PMID:30533525 PMID:31345272


    • An association has been curated linking SPG7 and genetic disease 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:11578209 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:21623769 PMID:22964162 PMID:25741868 PMID:27077743 PMID:28492532 PMID:34445196


    • An association has been curated linking SPG7 and genetic disease 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:11349599|RGD:126913929|RGD:13480713 (Homo sapiens) & RGD:11349599|RGD:126913929|RGD:13480713 (Homo sapiens) & RGD:11349599|RGD:126913929|RGD:13480713 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:26467025 PMID:28492532


    • An association has been curated linking SPG7 and genetic disease 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:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens) & RGD:10411155|RGD:10411728|RGD:13532304|RGD:155965411|RGD:156084594|RGD:156148017|RGD:156190837|RGD:156198653|RGD:156260550|RGD:156290286|RGD:329391884|RGD:329399560|RGD:401734328|RGD:401739913|RGD:401741038|RGD:401773584|RGD:401781243|RGD:401885668|RGD:401897977 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking SPG7 and genetic disease 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:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens) & RGD:10410191|RGD:12836796|RGD:12842424|RGD:13609963|RGD:150546820|RGD:151738209|RGD:151853971|RGD:155944416|RGD:156217683|RGD:156304079|RGD:156367353|RGD:26903426|RGD:28893309 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


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