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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking PAX8 and congenital nongoitrous hypothyroidism 2 in Canis lupus familiaris.        

  • 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 PAX8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital nongoitrous hypothyroidism 2  (DOID:0070124)
  • 0 papers in RGD have been used to annotate PAX8


  • An association has been curated linking PAX8 and congenital nongoitrous hypothyroidism 2 in Canis lupus familiaris.        

  • 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 PAX8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to congenital nongoitrous hypothyroidism 2  (DOID:0070124)
  • 0 papers in RGD have been used to annotate PAX8
  • Curation Notes: ClinVar Annotator: match by term: Hypothyroidism, congenital, nongoitrous, 2 | ClinVar Annotator: match by term: PAX8-related condition
  • Original References(s): PMID:11232006 PMID:11502839 PMID:12116225 PMID:15356023 PMID:15718293 PMID:17437516 PMID:17980011 PMID:20302910 PMID:23647375 PMID:25741868 PMID:28060725 PMID:28444304 PMID:28492532 PMID:29159607 PMID:30222900 PMID:9382140 PMID:9523167 PMID:9590296


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