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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Nkx2-5 and congenital nongoitrous hypothyroidism 5 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 NKX2-5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 37 papers in RGD have been used to annotate Nkx2-5


  • An association has been curated linking Nkx2-5 and congenital nongoitrous hypothyroidism 5 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 NKX2-5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 37 papers in RGD have been used to annotate Nkx2-5
  • Curation Notes: ClinVar Annotator: match by term: Hypothyroidism, congenital, nongoitrous, 5
  • Original References(s): PMID:16418214


  • An association has been curated linking Nkx2-5 and congenital nongoitrous hypothyroidism 5 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 NKX2-5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 37 papers in RGD have been used to annotate Nkx2-5
  • Curation Notes: ClinVar Annotator: match by term: Hypothyroidism, congenital, nongoitrous, 5
  • Original References(s): PMID:10587520 PMID:10903346 PMID:11714651 PMID:14607454 PMID:16418214 PMID:17891434 PMID:19073351 PMID:19464101 PMID:19533775 PMID:19948535 PMID:20456451 PMID:20807224 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Nkx2-5 and congenital nongoitrous hypothyroidism 5 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 NKX2-5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 37 papers in RGD have been used to annotate Nkx2-5
  • Curation Notes: ClinVar Annotator: match by term: Hypothyroidism, congenital, nongoitrous, 5
  • Original References(s): PMID:16418214 PMID:23285148 PMID:23661673 PMID:24376681 PMID:28492532


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