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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking Wdr13 and congenital disorder of glycosylation type IIm in Mus musculus.        

  • 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 WDR13 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 62 RGD objects have been annotated to congenital disorder of glycosylation type IIm  (DOID:0070265)
  • 7 papers in RGD have been used to annotate Wdr13
  • Curation Notes: ClinVar Annotator: match by term: DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 22 | ClinVar Annotator: match by term: SLC35A2-CDG
  • Original References(s): PMID:28492532


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