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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8595826 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:28492532 PMID:8490626


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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 familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8595822 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:2477392 PMID:3944267 PMID:7815420


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8595824 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:1971748 PMID:7815420


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8595827 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:8323539


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8595823 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:2592354


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8556895 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:3680515


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8595828 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:12783430


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8556897 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:1349286 PMID:3263393


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8556896 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:213719 PMID:3225819 PMID:3467353


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8595825 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:1628605 PMID:1782747 PMID:22135386 PMID:24788417 PMID:24886863 PMID:25741868 PMID:25910212 PMID:28492532 PMID:29100061 PMID:30197986 PMID:30686043 PMID:32861330 PMID:33111339 PMID:7923858


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:150490207 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:3192518


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:8595821 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29100061 PMID:30793526 PMID:33116287 PMID:3944271


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens) & RGD:11613679|RGD:11619752|RGD:11623939|RGD:11629343|RGD:11630902|RGD:11631099|RGD:11631147|RGD:11631287|RGD:11646542|RGD:11648401|RGD:11648599|RGD:11655012|RGD:11663279|RGD:28876491|RGD:28876498|RGD:28880392|RGD:329847270 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:15124261|RGD:28876502|RGD:28876510|RGD:28880389 (Homo sapiens) & RGD:15124261|RGD:28876502|RGD:28876510|RGD:28880389 (Homo sapiens) & RGD:15124261|RGD:28876502|RGD:28876510|RGD:28880389 (Homo sapiens) & RGD:15124261|RGD:28876502|RGD:28876510|RGD:28880389 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:28492532


    • An association has been curated linking APOC2 and familial apolipoprotein C-II 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:11628891|RGD:14695764|RGD:152982621 (Homo sapiens) & RGD:11628891|RGD:14695764|RGD:152982621 (Homo sapiens) & RGD:11628891|RGD:14695764|RGD:152982621 (Homo sapiens)
  • 2 RGD objects have been annotated to familial apolipoprotein C-II deficiency  (DOID:0111418)
  • 23 papers in RGD have been used to annotate APOC2
  • Curation Notes: ClinVar Annotator: match by term: Familial apolipoprotein C-II deficiency
  • Original References(s): PMID:25741868


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