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GENE - TERM ANNOTATION REPORT

27 Annotations Found.

An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by OMIM:612653
  • Original References(s): PMID:11380459 PMID:7530501


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by OMIM:612653
  • Original References(s): PMID:11380459


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by OMIM:612653
  • Original References(s): PMID:9734643


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by OMIM:612653
  • Original References(s): PMID:9973643


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by OMIM:612653
  • Original References(s): PMID:8567957


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:10745622 PMID:25741868


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:21039340 PMID:25741868 PMID:8471774


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:8011524 PMID:8547122


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:25741868


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:10942416 PMID:25741868 PMID:9207478


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:23255290 PMID:28492532 PMID:7812009


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:23255290 PMID:24033266 PMID:25741868 PMID:26879370 PMID:28492532


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:25741868 PMID:28492532 PMID:8206915


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:1419785 PMID:1520883 PMID:1678289 PMID:19229254 PMID:2146504 PMID:2196932 PMID:25741868 PMID:8608262 PMID:893429


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:28492532


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:25111073 PMID:26571219 PMID:28492532


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:8704215


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:11155072


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:1696010 PMID:2527366 PMID:8343110


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:25296721


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:25741868 PMID:9312167


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:16227998 PMID:7530501


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:8282779


  • An association has been curated linking Slc4a1 and hereditary spherocytosis type 4 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 SLC4A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 4  (DOID:0110919)
  • 44 papers in RGD have been used to annotate Slc4a1
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 4
  • Original References(s): PMID:1378323 PMID:25741868


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