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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by OMIM:300523
  • Original References(s): PMID:25741868


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by OMIM:300523
  • Original References(s): PMID:18414213


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by OMIM:300523
  • Original References(s): PMID:15889350, PMID:18187543


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by OMIM:300523
  • Original References(s): PMID:15980113, PMID:8484404


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by OMIM:300523
  • Original References(s): PMID:14661163


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by OMIM:300523


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by OMIM:300523
  • Original References(s): PMID:15889350, PMID:1605231, PMID:18187543


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by OMIM:300523
  • Original References(s): PMID:18414213, PMID:25741868


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by term: Allan-Herndon-Dudley syndrome
  • Original References(s): PMID:12871948


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by term: Allan-Herndon-Dudley syndrome
  • Original References(s): PMID:25167861


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by term: Allan-Herndon-Dudley syndrome
  • Original References(s): PMID:12871948, PMID:25741868


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by term: Allan-Herndon-Dudley syndrome
  • Original References(s): PMID:12871948, PMID:14661163, PMID:15889350, PMID:18398436, PMID:18414213, PMID:20628049, PMID:20655035, PMID:21098685, PMID:21896621, PMID:22805248, PMID:23550058, PMID:23568789, PMID:2393019, PMID:24265446, PMID:24629861, PMID:24665922, PMID:24721225, PMID:25527620, PMID:25644381, PMID:25741868, PMID:27212794, PMID:27672545, PMID:28492532


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by term: Allan-Herndon-Dudley syndrome
  • Original References(s): PMID:18414213, PMID:28492532


  • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley 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 SLC16A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Allan-Herndon-Dudley syndrome  (DOID:0050631)
  • 11 papers in RGD have been used to annotate Slc16a2
  • Curation Notes: ClinVar Annotator: match by term: MCT8 (SLC16A2)-Specific Thyroid Hormone Cell Transporter Deficiency
  • Original References(s): PMID:18414213, PMID:25741868, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.