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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking ICOSLG 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:151759451 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking ICOSLG 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:156223563 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking ICOSLG 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:13531600 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking ICOSLG 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:155982297 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking ICOSLG 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:329396412 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking ICOSLG 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:156104225 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking ICOSLG 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:151877362 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking ICOSLG 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:152137542 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking ICOSLG 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:156218521 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking ICOSLG 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:126735593 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking ICOSLG 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:401765670 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking ICOSLG 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:401866602 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate ICOSLG
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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