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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking C6 and complement component 6 deficiency 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:8602067 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:8690922


    • An association has been curated linking C6 and complement component 6 deficiency 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:42722789 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:10632667 PMID:12653841 PMID:17257682 PMID:22668955 PMID:25741868 PMID:28368462 PMID:28492532 PMID:8512929 PMID:9472666 PMID:9856498


    • An association has been curated linking C6 and complement component 6 deficiency in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6


    • An association has been curated linking C6 and complement component 6 deficiency 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:12849020 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:16199547 PMID:17257682 PMID:24378253 PMID:25741868 PMID:28492532 PMID:7535801 PMID:8871666


    • An association has been curated linking C6 and complement component 6 deficiency 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:126730417 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:10632667 PMID:17257682 PMID:22288589 PMID:23537992 PMID:25741868 PMID:28492532 PMID:9472666


    • An association has been curated linking C6 and complement component 6 deficiency 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:13528563 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:10632667 PMID:12653841 PMID:17257682 PMID:22288589 PMID:24033266 PMID:25741868 PMID:28492532 PMID:8512929 PMID:8690922 PMID:9472666 PMID:9856498


    • An association has been curated linking C6 and complement component 6 deficiency 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:151796793 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:17257682 PMID:25741868 PMID:28492532


    • An association has been curated linking C6 and complement component 6 deficiency 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:10401394 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:17257682 PMID:24033266 PMID:25741868 PMID:28492532 PMID:31440263


    • An association has been curated linking C6 and complement component 6 deficiency 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:42723659 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:31440263 PMID:9536098


    • An association has been curated linking C6 and complement component 6 deficiency 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:8562914 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:17257682 PMID:28492532 PMID:8512929 PMID:9856498


    • An association has been curated linking C6 and complement component 6 deficiency 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:21072260 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:17257682 PMID:25741868 PMID:28492532 PMID:32860008


    • An association has been curated linking C6 and complement component 6 deficiency in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking C6 and complement component 6 deficiency 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:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens) & RGD:127305524|RGD:127305529|RGD:127319509|RGD:12849173|RGD:15171878|RGD:151782831|RGD:151804379|RGD:15192755|RGD:21069081|RGD:41405869 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking C6 and complement component 6 deficiency 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:126733000|RGD:152061886|RGD:401723998 (Homo sapiens) & RGD:126733000|RGD:152061886|RGD:401723998 (Homo sapiens) & RGD:126733000|RGD:152061886|RGD:401723998 (Homo sapiens)
  • 2 RGD objects have been annotated to complement component 6 deficiency  (DOID:0060299)
  • 13 papers in RGD have been used to annotate C6
  • Curation Notes: ClinVar Annotator: match by term: Complement component 6 deficiency
  • Original References(s): PMID:25741868


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