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1 Annotations Found.

An association has been curated linking Hcn4 and genetic disease in Heterocephalus glaber.        

  • The association was inferred from sequence orthology (ISO)
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:13531607 (Homo sapiens)
  • 0 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate Hcn4
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:12750403, PMID:1309182, PMID:15123648, PMID:16407510, PMID:17646576, PMID:19165230, PMID:21220308, PMID:21615589, PMID:22481543, PMID:22840528, PMID:23178648, PMID:24569893, PMID:25145517

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