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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking GP1BB and DiGeorge syndrome 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:13819482 (Homo sapiens)
  • 243 RGD objects have been annotated to DiGeorge syndrome  (DOID:11198)
  • 11 papers in RGD have been used to annotate GP1BB
  • Curation Notes: ClinVar Annotator: match by term: DiGeorge syndrome
  • Original References(s): PMID:25516202 PMID:28492532


    • An association has been curated linking GP1BB and DiGeorge syndrome 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:127240024 (Homo sapiens)
  • 243 RGD objects have been annotated to DiGeorge syndrome  (DOID:11198)
  • 11 papers in RGD have been used to annotate GP1BB
  • Curation Notes: ClinVar Annotator: match by term: DiGeorge syndrome
  • Original References(s): PMID:24826987 PMID:25205790 PMID:25516202 PMID:25860641 PMID:26805781 PMID:26805782 PMID:28492532 PMID:29500247 PMID:30245509


    • An association has been curated linking GP1BB and DiGeorge syndrome 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:21404924 (Homo sapiens)
  • 243 RGD objects have been annotated to DiGeorge syndrome  (DOID:11198)
  • 11 papers in RGD have been used to annotate GP1BB
  • Curation Notes: ClinVar Annotator: match by term: DiGeorge syndrome
  • Original References(s): PMID:32581362


    • An association has been curated linking GP1BB and DiGeorge syndrome 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:329349407 (Homo sapiens)
  • 243 RGD objects have been annotated to DiGeorge syndrome  (DOID:11198)
  • 11 papers in RGD have been used to annotate GP1BB
  • Curation Notes: ClinVar Annotator: match by term: 22q11.2 deletion syndrome


    • An association has been curated linking GP1BB and DiGeorge syndrome 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:127234734|RGD:127234753 (Homo sapiens) & RGD:127234734|RGD:127234753 (Homo sapiens)
  • 243 RGD objects have been annotated to DiGeorge syndrome  (DOID:11198)
  • 11 papers in RGD have been used to annotate GP1BB
  • Curation Notes: ClinVar Annotator: match by term: DiGeorge syndrome
  • Original References(s): PMID:31690835


    • An association has been curated linking GP1BB and DiGeorge syndrome 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:151807981|RGD:26905953 (Homo sapiens) & RGD:151807981|RGD:26905953 (Homo sapiens)
  • 243 RGD objects have been annotated to DiGeorge syndrome  (DOID:11198)
  • 11 papers in RGD have been used to annotate GP1BB
  • Curation Notes: ClinVar Annotator: match by term: DiGeorge syndrome
  • Original References(s): PMID:28492532


    • An association has been curated linking GP1BB and DiGeorge syndrome 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:13486665|RGD:13611829|RGD:26907185 (Homo sapiens) & RGD:13486665|RGD:13611829|RGD:26907185 (Homo sapiens) & RGD:13486665|RGD:13611829|RGD:26907185 (Homo sapiens)
  • 243 RGD objects have been annotated to DiGeorge syndrome  (DOID:11198)
  • 11 papers in RGD have been used to annotate GP1BB
  • Curation Notes: ClinVar Annotator: match by term: DiGeorge syndrome
  • Original References(s): PMID:24826987 PMID:25205790 PMID:25516202 PMID:28492532


    • An association has been curated linking GP1BB and DiGeorge syndrome 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:151796486|RGD:26907831 (Homo sapiens) & RGD:151796486|RGD:26907831 (Homo sapiens)
  • 243 RGD objects have been annotated to DiGeorge syndrome  (DOID:11198)
  • 11 papers in RGD have been used to annotate GP1BB
  • Curation Notes: ClinVar Annotator: match by term: DiGeorge syndrome
  • Original References(s): PMID:21921585 PMID:25516202 PMID:28492532


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