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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking VANGL1 and caudal regression syndrome in Canis lupus familiaris.        

  • 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 VANGL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to caudal regression syndrome  (DOID:0080700)
  • 0 papers in RGD have been used to annotate VANGL1
  • Qualifier: susceptibility


    • An association has been curated linking VANGL1 and caudal regression 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 VANGL1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 RGD objects have been annotated to caudal regression syndrome  (DOID:0080700)
  • 0 papers in RGD have been used to annotate VANGL1
  • Curation Notes: ClinVar Annotator: match by term: Caudal regression sequence | ClinVar Annotator: match by term: Sacral defect with anterior meningocele
  • Original References(s): PMID:17409324 PMID:19319979 PMID:22892949 PMID:24033266 PMID:24307374 PMID:24407469 PMID:24452931 PMID:24838524 PMID:25068569 PMID:25208524 PMID:25741868 PMID:26196381 PMID:28492532


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