Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

GENE - TERM ANNOTATION REPORT

19 Annotations Found.

An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:8560839 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:28492532


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:8560840 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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 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:8560829 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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 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:151828237 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:25741868 PMID:28492532 PMID:29368431


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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 5  (DOID:0070125)
  • 24 papers in RGD have been used to annotate NKX2-5


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:8568123 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:21110066 PMID:25741868 PMID:25742962 PMID:27152669 PMID:28492532 PMID:30508507 PMID:31824610 PMID:31983221 PMID:32425884


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:8560831 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:11714651 PMID:25741868


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:9683164 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:12074273 PMID:18414213 PMID:22920929 PMID:25741868 PMID:28492532


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:13464695 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:14607454 PMID:17544441 PMID:25741868 PMID:28492532


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:12741223 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:24376681 PMID:25741868 PMID:26805889 PMID:27904570 PMID:28492532 PMID:28536625


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:8560832 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:11714651 PMID:15161646 PMID:15917268 PMID:25741868 PMID:28492532


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:13529881 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:19933292 PMID:25741868 PMID:27152669 PMID:28492532


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:13535609 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:12798584 PMID:14607454 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 papers in RGD have been used to annotate NKX2-5
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:151866719 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:28492532


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:13813788|RGD:26886495 (Homo sapiens) & RGD:13813788|RGD:26886495 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:14607454 PMID:25741868 PMID:28492532


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:150546084|RGD:150557099 (Homo sapiens) & RGD:150546084|RGD:150557099 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:25741868


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:11638003|RGD:26897890 (Homo sapiens) & RGD:11638003|RGD:26897890 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:25741868 PMID:28492532 PMID:32369864


    • An association has been curated linking NKX2-5 and congenital nongoitrous hypothyroidism 5 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:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens) & RGD:10044673|RGD:10044925|RGD:126735383|RGD:126735649|RGD:126735772|RGD:126735800|RGD:126735901|RGD:12841058|RGD:12842710|RGD:13527753|RGD:13531474|RGD:13541982|RGD:13809246|RGD:14742792|RGD:151765558|RGD:151823939|RGD:26891986|RGD:26901542|RGD:26915328|RGD:38486623 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital nongoitrous hypothyroidism 5  (DOID:0070125)
  • 24 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:25741868 PMID:28492532


    • Go Back to source page   Continue to Ontology report