Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 2
  • Original References(s): PMID:11703334 PMID:25741868


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 2
  • Original References(s): PMID:25741868 PMID:7883966


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 2
  • Original References(s): PMID:25741868


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spectrin kissimmee
  • Original References(s): PMID:6215583 PMID:8102379


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 2


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 2
  • Original References(s): PMID:9414314


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spectrin durham
  • Original References(s): PMID:1385736 PMID:3654760


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 2
  • Original References(s): PMID:25741868 PMID:9714702


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 2
  • Original References(s): PMID:19538529 PMID:25741868


  • An association has been curated linking Sptb and hereditary spherocytosis type 2 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 SPTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hereditary spherocytosis type 2  (DOID:0110917)
  • 7 papers in RGD have been used to annotate Sptb
  • Curation Notes: ClinVar Annotator: match by term: Spherocytosis type 2
  • Original References(s): PMID:25741868 PMID:7883966 PMID:8844207


  • Go Back to source page   Continue to Ontology report