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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Acox1 and peroxisomal acyl-CoA oxidase 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 ACOX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to peroxisomal acyl-CoA oxidase deficiency  (DOID:0050797)
  • 14 papers in RGD have been used to annotate Acox1


    • An association has been curated linking Acox1 and peroxisomal acyl-CoA oxidase deficiency in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Acox1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to peroxisomal acyl-CoA oxidase deficiency  (DOID:0050797)
  • 14 papers in RGD have been used to annotate Acox1
  • Curation Notes: OMIM:264470


    • An association has been curated linking Acox1 and peroxisomal acyl-CoA oxidase 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 ACOX1 (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to peroxisomal acyl-CoA oxidase deficiency  (DOID:0050797)
  • 14 papers in RGD have been used to annotate Acox1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Acox1 and peroxisomal acyl-CoA oxidase 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 ACOX1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to peroxisomal acyl-CoA oxidase deficiency  (DOID:0050797)
  • 14 papers in RGD have been used to annotate Acox1
  • Curation Notes: ClinVar Annotator: match by term: Peroxisomal acyl-CoA oxidase deficiency | ClinVar Annotator: match by term: Pseudoneonatal adrenoleukodystrophy
  • Original References(s): PMID:11815777 PMID:16199547 PMID:16773508 PMID:17458872 PMID:17576681 PMID:18536048 PMID:20185470 PMID:24033266 PMID:25326637 PMID:25640679 PMID:25741868 PMID:26965209 PMID:28492532 PMID:2894756 PMID:30561787 PMID:31130284 PMID:32169171 PMID:33510602 PMID:8040306 PMID:8279468 PMID:9536098


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