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GENE - TERM ANNOTATION REPORT

4 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 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 CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC16A2 (Homo sapiens) [(EXP) inferred from experiment]
  • 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: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Slc16a2 and Allan-Herndon-Dudley syndrome in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Slc16a2 (Mus musculus) [(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: 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 term: Allan-Herndon-Dudley syndrome | ClinVar Annotator: match by term: Mental retardation and muscular atrophy
  • Original References(s): PMID:12871948 PMID:14661163 PMID:15488219 PMID:15889350 PMID:15980113 PMID:1605231 PMID:16417886 PMID:16957765 PMID:17356046 PMID:18187543 PMID:18398436 PMID:18414213 PMID:18636565 PMID:20083155 PMID:20301789 PMID:21836662 PMID:23568789 PMID:23744248 PMID:24265446 PMID:24721225 PMID:25167861 PMID:25517855 PMID:25527620 PMID:25741868 PMID:27081503 PMID:27212794 PMID:27805744 PMID:28492532 PMID:30369548 PMID:31127274 PMID:31410843 PMID:31585110 PMID:31690835 PMID:32277047 PMID:32559475 PMID:33504798 PMID:33847015 PMID:33860439 PMID:8484404


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