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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking TBL1X and congenital nongoitrous hypothyroidism 8 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 8  (DOID:0111837)
  • 4 papers in RGD have been used to annotate TBL1X


    • An association has been curated linking TBL1X and congenital nongoitrous hypothyroidism 8 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:14976020 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 8  (DOID:0111837)
  • 4 papers in RGD have been used to annotate TBL1X
  • Curation Notes: ClinVar Annotator: match by term: Hypothyroidism, congenital, nongoitrous, 8
  • Original References(s): PMID:25741868 PMID:30591955


    • An association has been curated linking TBL1X and congenital nongoitrous hypothyroidism 8 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:150503288|RGD:151352716|RGD:151353070|RGD:151353071|RGD:155800801|RGD:401921469 (Homo sapiens) & RGD:150503288|RGD:151352716|RGD:151353070|RGD:151353071|RGD:155800801|RGD:401921469 (Homo sapiens) & RGD:150503288|RGD:151352716|RGD:151353070|RGD:151353071|RGD:155800801|RGD:401921469 (Homo sapiens) & RGD:150503288|RGD:151352716|RGD:151353070|RGD:151353071|RGD:155800801|RGD:401921469 (Homo sapiens) & RGD:150503288|RGD:151352716|RGD:151353070|RGD:151353071|RGD:155800801|RGD:401921469 (Homo sapiens) & RGD:150503288|RGD:151352716|RGD:151353070|RGD:151353071|RGD:155800801|RGD:401921469 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 8  (DOID:0111837)
  • 4 papers in RGD have been used to annotate TBL1X
  • Curation Notes: ClinVar Annotator: match by term: Hypothyroidism, congenital, nongoitrous, 8
  • Original References(s): PMID:25741868


    • An association has been curated linking TBL1X and congenital nongoitrous hypothyroidism 8 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:14976017|RGD:14976018|RGD:14976019|RGD:26903614|RGD:26903615 (Homo sapiens) & RGD:14976017|RGD:14976018|RGD:14976019|RGD:26903614|RGD:26903615 (Homo sapiens) & RGD:14976017|RGD:14976018|RGD:14976019|RGD:26903614|RGD:26903615 (Homo sapiens) & RGD:14976017|RGD:14976018|RGD:14976019|RGD:26903614|RGD:26903615 (Homo sapiens) & RGD:14976017|RGD:14976018|RGD:14976019|RGD:26903614|RGD:26903615 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 8  (DOID:0111837)
  • 4 papers in RGD have been used to annotate TBL1X
  • Curation Notes: ClinVar Annotator: match by term: Hypothyroidism, congenital, nongoitrous, 8
  • Original References(s): PMID:25741868 PMID:27603907


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