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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking H1f4 and Rahman Syndrome 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 H1-4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rahman Syndrome  (DOID:9002839)
  • 4 papers in RGD have been used to annotate H1f4
  • Curation Notes: ClinVar Annotator: match by term: RAHMAN SYNDROME
  • Original References(s): PMID:28475857


    • An association has been curated linking H1f4 and Rahman Syndrome 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 H1-4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rahman Syndrome  (DOID:9002839)
  • 4 papers in RGD have been used to annotate H1f4
  • Curation Notes: ClinVar Annotator: match by term: RAHMAN SYNDROME
  • Original References(s): PMID:25741868


    • An association has been curated linking H1f4 and Rahman Syndrome 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 H1-4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rahman Syndrome  (DOID:9002839)
  • 4 papers in RGD have been used to annotate H1f4


    • An association has been curated linking H1f4 and Rahman Syndrome 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 H1-4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rahman Syndrome  (DOID:9002839)
  • 4 papers in RGD have been used to annotate H1f4
  • Curation Notes: ClinVar Annotator: match by term: RAHMAN SYNDROME


    • An association has been curated linking H1f4 and Rahman Syndrome 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 H1-4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rahman Syndrome  (DOID:9002839)
  • 4 papers in RGD have been used to annotate H1f4
  • Curation Notes: ClinVar Annotator: match by term: RAHMAN SYNDROME
  • Original References(s): PMID:25741868 PMID:28475857


    • An association has been curated linking H1f4 and Rahman Syndrome 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 H1-4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Rahman Syndrome  (DOID:9002839)
  • 4 papers in RGD have been used to annotate H1f4
  • Curation Notes: ClinVar Annotator: match by term: RAHMAN SYNDROME
  • Original References(s): PMID:23945933 PMID:25081361 PMID:25741868 PMID:25741869 PMID:28475857


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