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GENE - TERM ANNOTATION REPORT

23 Annotations Found.

An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:23453696, PMID:28492532


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:28492532


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19621418, PMID:28492532


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:20941788


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:28492532, PMID:29901818


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605, PMID:19621418


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605, PMID:28492532


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:21252497, PMID:28492532, PMID:29031773


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: CDA II
  • Original References(s): PMID:26522472, PMID:28492532


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605, PMID:19621418, PMID:20015893, PMID:20941788, PMID:23453696


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605, PMID:20015893


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605, PMID:19621418, PMID:20015893, PMID:21850656, PMID:28492532


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605, PMID:19621418, PMID:20015893, PMID:21252497, PMID:21850656, PMID:22208203, PMID:25044164, PMID:28492532, PMID:30311386


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:22428539, PMID:25741868, PMID:28492532


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: HEMPAS anemia
  • Original References(s): PMID:19561605, PMID:19621418, PMID:25044164, PMID:28492532, PMID:30311386


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:25741868


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605, PMID:25741868


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:19561605, PMID:32581362


  • An association has been curated linking Sec23b and congenital dyserythropoietic anemia type II 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 SEC23B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital dyserythropoietic anemia type II  (DOID:0111401)
  • 6 papers in CRRD have been used to annotate Sec23b
  • Curation Notes: ClinVar Annotator: match by term: Congenital dyserythropoietic anemia, type II
  • Original References(s): PMID:32581362


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