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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:26184105, PMID:27239559, PMID:28492532, PMID:29237733


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:23332920, PMID:24570283, PMID:28492532


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:22190180, PMID:25918394, PMID:28492532


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:25326555, PMID:28492532


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:24591628, PMID:24619930, PMID:25044882, PMID:25577287, PMID:25741868, PMID:26436962, PMID:28492532, PMID:28624464, PMID:4085141


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:27066587, PMID:28492532


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:24492416, PMID:28492532


  • An association has been curated linking Stim1 and Stormorken syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with STIM1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Stormorken syndrome  (DOID:0060354)
  • 11 papers in CRRD have been used to annotate Stim1
  • Curation Notes: ClinVar Annotator: match by term: Stormorken syndrome
  • Original References(s): PMID:12623447, PMID:12745453, PMID:12944247, PMID:12944248, PMID:24570283, PMID:25577287, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.