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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Mipep and combined oxidative phosphorylation deficiency 31 in Mus musculus.        

  • 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 MIPEP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to combined oxidative phosphorylation deficiency 31  (DOID:0111488)
  • 6 papers in RGD have been used to annotate Mipep


    • An association has been curated linking Mipep and combined oxidative phosphorylation deficiency 31 in Mus musculus.        

  • 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 MIPEP (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to combined oxidative phosphorylation deficiency 31  (DOID:0111488)
  • 6 papers in RGD have been used to annotate Mipep
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Mipep and combined oxidative phosphorylation deficiency 31 in Mus musculus.        

  • 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 MIPEP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to combined oxidative phosphorylation deficiency 31  (DOID:0111488)
  • 6 papers in RGD have been used to annotate Mipep
  • Curation Notes: ClinVar Annotator: match by term: Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome
  • Original References(s): PMID:16199547 PMID:24033266 PMID:25741868 PMID:26762739 PMID:27799064 PMID:28492532 PMID:33587123 PMID:34620555


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