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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking ADAR and dyschromatosis symmetrica hereditaria in Sus scrofa.        

  • 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 ADAR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to dyschromatosis symmetrica hereditaria  (DOID:0060257)
  • 0 papers in RGD have been used to annotate ADAR
  • Curation Notes: ClinVar Annotator: match by term: Symmetrical dyschromatosis of extremities
  • Original References(s): PMID:12916015 PMID:15102079 PMID:15146470 PMID:15347341 PMID:15489923 PMID:15659327 PMID:15955093 PMID:16199547 PMID:16536805 PMID:16817193 PMID:16917490 PMID:16935814 PMID:17225010 PMID:17569068 PMID:17576681 PMID:18705826 PMID:19017046 PMID:19060901 PMID:20069304 PMID:20186421 PMID:20300939 PMID:20301648 PMID:20430589 PMID:20439151 PMID:21182352 PMID:21211811 PMID:21924887 PMID:21933234 PMID:22336994 PMID:22974014 PMID:23001123 PMID:24033266 PMID:24262145 PMID:24950769 PMID:25243380 PMID:25326637 PMID:25456137 PMID:25468572 PMID:25604658 PMID:25640679 PMID:25741868 PMID:25982145 PMID:26372505 PMID:26629815 PMID:26802932 PMID:26892242 PMID:27937139 PMID:28139822 PMID:28492532 PMID:28502085 PMID:28561207 PMID:29185800 PMID:29221912 PMID:29536976 PMID:29603717 PMID:29691679 PMID:29775506 PMID:29896739 PMID:29915444 PMID:30564185 PMID:30692772 PMID:30755392 PMID:31423758 PMID:31772029 PMID:32593192 PMID:32801363 PMID:32996714 PMID:33289110 PMID:33307271 PMID:33723056 PMID:34343497 PMID:34702576 PMID:34988976 PMID:35551623 PMID:35859177 PMID:8627722 PMID:9536098 PMID:9889202


  • An association has been curated linking ADAR and dyschromatosis symmetrica hereditaria in Sus scrofa.        

  • 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 ADAR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to dyschromatosis symmetrica hereditaria  (DOID:0060257)
  • 0 papers in RGD have been used to annotate ADAR


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