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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking Slc19a2 and 1q24 Deletion Syndrome in Heterocephalus glaber.        

  • 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 SLC19A2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 88 RGD objects have been annotated to 1q24 Deletion Syndrome  (DOID:9007734)
  • 0 papers in RGD have been used to annotate Slc19a2
  • Curation Notes: ClinVar Annotator: match by term: 1q24q25 microdeletion syndrome
  • Original References(s): PMID:25741868


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