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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: Dystonia 28, childhood-onset


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: DYSTONIA 28, CHILDHOOD-ONSET
  • Original References(s): PMID:27839873


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: DYSTONIA 28, CHILDHOOD-ONSET
  • Original References(s): PMID:27992417


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: Dystonia 28, childhood-onset
  • Original References(s): PMID:25741878


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: Dystonia 28, childhood-onset
  • Original References(s): PMID:25741868, PMID:32860008


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: Dystonia 28, childhood-onset
  • Original References(s): PMID:25741868


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: Dystonia 28, childhood-onset
  • Original References(s): PMID:25741868, PMID:27839873


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: Dystonia 28, childhood-onset
  • Original References(s): PMID:25741868, PMID:27992417


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: Dystonia 28, childhood-onset
  • Original References(s): PMID:28520167, PMID:29697234


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b


  • An association has been curated linking Kmt2b and DYSTONIA 28, CHILDHOOD-ONSET 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 KMT2B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to DYSTONIA 28, CHILDHOOD-ONSET  (DOID:9004049)
  • 11 papers in CRRD have been used to annotate Kmt2b
  • Curation Notes: ClinVar Annotator: match by term: Dystonia 28, childhood-onset
  • Original References(s): PMID:25741868, PMID:27992417, 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.