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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Slc46a1 and hereditary folate malabsorption in Heterocephalus glaber.        

  • 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 SLC46A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hereditary folate malabsorption  (DOID:0111678)
  • 0 papers in RGD have been used to annotate Slc46a1


    • An association has been curated linking Slc46a1 and hereditary folate malabsorption 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 SLC46A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hereditary folate malabsorption  (DOID:0111678)
  • 0 papers in RGD have been used to annotate Slc46a1
  • Curation Notes: ClinVar Annotator: match by term: Congenital defect of folate absorption | ClinVar Annotator: match by term: Hereditary Folate Malabsorption
  • Original References(s): PMID:11804211 PMID:11807405 PMID:17129779 PMID:17446347 PMID:18559978 PMID:19176287 PMID:19740703 PMID:20301716 PMID:20686069 PMID:20795774 PMID:21333572 PMID:21489556 PMID:21602279 PMID:22345511 PMID:22843796 PMID:24534056 PMID:25167861 PMID:25504888 PMID:25741868 PMID:27664775 PMID:28492532 PMID:28685492 PMID:3987728


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