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1 Annotations Found.

An association has been curated linking SFMBT2 and hypoparathyroidism-deafness-renal disease syndrome in Canis lupus familiaris.        

  • 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:14350360 (Homo sapiens)
  • 66 CRRD objects have been annotated to hypoparathyroidism-deafness-renal disease syndrome  (DOID:0060878)
  • 0 papers in CRRD have been used to annotate SFMBT2
  • Curation Notes: ClinVar Annotator: match by term: Barakat syndrome
  • Original References(s): PMID:25741868

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