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GENE - TERM ANNOTATION REPORT

56 Annotations Found.

An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:21637106 PMID:24399159 PMID:24922459 PMID:25741868


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:22019127 PMID:24036952 PMID:25741868 PMID:25944730 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:18272325 PMID:25741868 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:21086191 PMID:21984974 PMID:24036952 PMID:24055113 PMID:25741868 PMID:25758994 PMID:25834947 PMID:26017485 PMID:26332594 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:2049575 PMID:21086191 PMID:24033266 PMID:25637381 PMID:25741868 PMID:25758994 PMID:25846194 PMID:27011056 PMID:27964749 PMID:28492532 PMID:28748566 PMID:30374176


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:22019127 PMID:24033266 PMID:25503501 PMID:25741868 PMID:26188975 PMID:28492532 PMID:8514866


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:22019127 PMID:24055113 PMID:25637381 PMID:25741868 PMID:26332594 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:2235526 PMID:24033266 PMID:25741868


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:25834947 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:19344236 PMID:24922459 PMID:25758994 PMID:28492532 PMID:29543232 PMID:30793832 PMID:30919682 PMID:7695699 PMID:8218237 PMID:8990011


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:22001912 PMID:24033266 PMID:25637381 PMID:25741868 PMID:25834947 PMID:27888582 PMID:28492532 PMID:30115950


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:24055113 PMID:25637381 PMID:25741868 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25637381 PMID:25741868 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:19424605 PMID:22019127 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:24033266


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:25758994 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • The association was inferred from electronic annotation (IEA)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: OMIM:130050


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:17053184 PMID:19344236 PMID:22713205 PMID:23234825 PMID:24922459 PMID:25741868 PMID:25758994 PMID:28492532 PMID:7695699 PMID:8218237


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:27153395 PMID:28492532 PMID:30379966


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:25758994 PMID:26854089 PMID:28087566 PMID:28492532 PMID:29590070 PMID:30087447 PMID:31531849


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:24922459 PMID:25758994


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:18043893 PMID:21533953 PMID:24922459 PMID:25758994 PMID:28492532 PMID:8881656 PMID:9036918 PMID:9399899


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10923041 PMID:24922459


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:24922459


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:19344236 PMID:20052764 PMID:24033266 PMID:24922459 PMID:25758994 PMID:28492532 PMID:7695699 PMID:8218237


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:23148498 PMID:25741868 PMID:27011056 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:25741868


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:19344236 PMID:24922459 PMID:25741868 PMID:25758994 PMID:28492532 PMID:29778910 PMID:7695699 PMID:8218237


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:19344236 PMID:21086191 PMID:21520333 PMID:24922459 PMID:25741868 PMID:25758994 PMID:28492532 PMID:30115950 PMID:7695699 PMID:8218237


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:19344236 PMID:24922459 PMID:25741868 PMID:25758994 PMID:28492532 PMID:7695699 PMID:8218237


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:22001912 PMID:25741868 PMID:25776230 PMID:26332594 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:22019127 PMID:24922459 PMID:30474650 PMID:31126764


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:17576681 PMID:28492532 PMID:30999998 PMID:9536098


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:24922459 PMID:25741868 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:2349939 PMID:24399159 PMID:24922459 PMID:25741868 PMID:27306637 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:24922459 PMID:25741868


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:26017485 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:25846194 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:18043893 PMID:19344236 PMID:24922459 PMID:25741868 PMID:25758994 PMID:28492532 PMID:7695699 PMID:8218237


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:28492532 PMID:28655553


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:18272325 PMID:24033266 PMID:25741868


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:25944730 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:22001912 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:25758994 PMID:28492532 PMID:30122538


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31719132


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:19011090 PMID:24922459 PMID:28492532 PMID:7695699


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:10706896 PMID:16751282 PMID:24922459 PMID:25758994


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:24951259 PMID:25741868 PMID:28492532 PMID:31719132


  • An association has been curated linking Col3a1 and vascular type Ehlers-Danlos syndrome in Mus musculus.        

  • 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 COL3A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to vascular type Ehlers-Danlos syndrome  (DOID:14756)
  • 30 papers in RGD have been used to annotate Col3a1
  • Curation Notes: ClinVar Annotator: match by term: Ehlers Danlos syndrome, Sack-Barabas type
  • Original References(s): PMID:28492532 PMID:29510914


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