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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking STX1B 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:40886640 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18691641 PMID:30737342


    • An association has been curated linking STX1B 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:13830646 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25362483 PMID:25741868 PMID:28492532 PMID:30737342


    • An association has been curated linking STX1B 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:40886562 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532 PMID:30737342


    • An association has been curated linking STX1B 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:11560184 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30737342


    • An association has been curated linking STX1B 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:13493451|RGD:15162499|RGD:38491835 (Homo sapiens) & RGD:13493451|RGD:15162499|RGD:38491835 (Homo sapiens) & RGD:13493451|RGD:15162499|RGD:38491835 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking STX1B 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:13473585|RGD:13624684|RGD:13829945|RGD:151823053|RGD:155729137|RGD:26917338 (Homo sapiens) & RGD:13473585|RGD:13624684|RGD:13829945|RGD:151823053|RGD:155729137|RGD:26917338 (Homo sapiens) & RGD:13473585|RGD:13624684|RGD:13829945|RGD:151823053|RGD:155729137|RGD:26917338 (Homo sapiens) & RGD:13473585|RGD:13624684|RGD:13829945|RGD:151823053|RGD:155729137|RGD:26917338 (Homo sapiens) & RGD:13473585|RGD:13624684|RGD:13829945|RGD:151823053|RGD:155729137|RGD:26917338 (Homo sapiens) & RGD:13473585|RGD:13624684|RGD:13829945|RGD:151823053|RGD:155729137|RGD:26917338 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking STX1B 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:13532653|RGD:13830464|RGD:155676646|RGD:155726587|RGD:155740641|RGD:156060627|RGD:401737978 (Homo sapiens) & RGD:13532653|RGD:13830464|RGD:155676646|RGD:155726587|RGD:155740641|RGD:156060627|RGD:401737978 (Homo sapiens) & RGD:13532653|RGD:13830464|RGD:155676646|RGD:155726587|RGD:155740641|RGD:156060627|RGD:401737978 (Homo sapiens) & RGD:13532653|RGD:13830464|RGD:155676646|RGD:155726587|RGD:155740641|RGD:156060627|RGD:401737978 (Homo sapiens) & RGD:13532653|RGD:13830464|RGD:155676646|RGD:155726587|RGD:155740641|RGD:156060627|RGD:401737978 (Homo sapiens) & RGD:13532653|RGD:13830464|RGD:155676646|RGD:155726587|RGD:155740641|RGD:156060627|RGD:401737978 (Homo sapiens) & RGD:13532653|RGD:13830464|RGD:155676646|RGD:155726587|RGD:155740641|RGD:156060627|RGD:401737978 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking STX1B 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:401747459 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


    • An association has been curated linking STX1B 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:13473717 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:26467025 PMID:28492532


    • An association has been curated linking STX1B 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:13624652|RGD:13801926|RGD:13801931 (Homo sapiens) & RGD:13624652|RGD:13801926|RGD:13801931 (Homo sapiens) & RGD:13624652|RGD:13801926|RGD:13801931 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate STX1B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


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