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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Slc25a15 and ornithine translocase deficiency in Rattus norvegicus.        

  • 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 SLC25A15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to ornithine translocase deficiency  (DOID:0050720)
  • 11 papers in RGD have been used to annotate Slc25a15


    • An association has been curated linking Slc25a15 and ornithine translocase deficiency in Rattus norvegicus.        

  • 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 SLC25A15 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to ornithine translocase deficiency  (DOID:0050720)
  • 11 papers in RGD have been used to annotate Slc25a15
  • Curation Notes: ClinVar Annotator: match by term: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | ClinVar Annotator: match by term: Ornithine translocase deficiency
  • Original References(s): PMID:10369256 PMID:10805333 PMID:11355015 PMID:11552031 PMID:11668643 PMID:12807890 PMID:14759633 PMID:16199547 PMID:16376511 PMID:16601889 PMID:16940241 PMID:17576681 PMID:17825324 PMID:18376250 PMID:18406340 PMID:18666241 PMID:18978333 PMID:19242930 PMID:22292090 PMID:22649802 PMID:23430880 PMID:24473688 PMID:25741868 PMID:25818551 PMID:25874378 PMID:26589310 PMID:28492532 PMID:29554876 PMID:30187369 PMID:30243302 PMID:31443672 PMID:31589614 PMID:32214227 PMID:32340404 PMID:3407856 PMID:9536098


    • An association has been curated linking Slc25a15 and ornithine translocase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC25A15 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to ornithine translocase deficiency  (DOID:0050720)
  • 11 papers in RGD have been used to annotate Slc25a15
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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