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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking TXNDC2 and chromosome 18p deletion syndrome in Canis lupus familiaris.        

  • 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 TXNDC2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 49 RGD objects have been annotated to chromosome 18p deletion syndrome  (DOID:0060406)
  • 0 papers in RGD have been used to annotate TXNDC2
  • Curation Notes: ClinVar Annotator: match by term: Del(18p) syndrome
  • Original References(s): PMID:31690835


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