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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Rmnd1 and combined oxidative phosphorylation deficiency 11 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 RMND1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to combined oxidative phosphorylation deficiency 11  (DOID:0111481)
  • 5 papers in RGD have been used to annotate Rmnd1


    • An association has been curated linking Rmnd1 and combined oxidative phosphorylation deficiency 11 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 RMND1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to combined oxidative phosphorylation deficiency 11  (DOID:0111481)
  • 5 papers in RGD have been used to annotate Rmnd1
  • Curation Notes: ClinVar Annotator: match by term: Combined oxidative phosphorylation deficiency 11
  • Original References(s): PMID:18835491 PMID:23022098 PMID:23022099 PMID:24033266 PMID:25058219 PMID:25326635 PMID:25604853 PMID:25741868 PMID:25741914 PMID:26238252 PMID:26395190 PMID:27159321 PMID:27350610 PMID:27412952 PMID:27843092 PMID:28492532 PMID:29071585 PMID:31506229 PMID:31568715 PMID:31981491 PMID:32576985


    • An association has been curated linking Rmnd1 and combined oxidative phosphorylation deficiency 11 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 RMND1 (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to combined oxidative phosphorylation deficiency 11  (DOID:0111481)
  • 5 papers in RGD have been used to annotate Rmnd1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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