Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Coq8a and primary coenzyme Q10 deficiency 4 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 COQ8A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to primary coenzyme Q10 deficiency 4  (DOID:0070241)
  • 6 papers in RGD have been used to annotate Coq8a


    • An association has been curated linking Coq8a and primary coenzyme Q10 deficiency 4 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 COQ8A (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to primary coenzyme Q10 deficiency 4  (DOID:0070241)
  • 6 papers in RGD have been used to annotate Coq8a
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Coq8a and primary coenzyme Q10 deficiency 4 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 Coq8a (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to primary coenzyme Q10 deficiency 4  (DOID:0070241)
  • 6 papers in RGD have been used to annotate Coq8a
  • Curation Notes: OMIM:612016


    • An association has been curated linking Coq8a and primary coenzyme Q10 deficiency 4 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 COQ8A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to primary coenzyme Q10 deficiency 4  (DOID:0070241)
  • 6 papers in RGD have been used to annotate Coq8a
  • Curation Notes: ClinVar Annotator: match by term: COQ8A-related condition | ClinVar Annotator: match by term: Coenzyme Q10 deficiency, primary, 4 | ClinVar Annotator: match by term: Spinocerebellar ataxia, autosomal recessive 9
  • Original References(s): PMID:12682339 PMID:15326254 PMID:16199547 PMID:17576681 PMID:18319072 PMID:18319074 PMID:18414213 PMID:19440741 PMID:20495179 PMID:20580948 PMID:21873089 PMID:22036850 PMID:24033266 PMID:24048965 PMID:24164873 PMID:24218524 PMID:25131622 PMID:25280894 PMID:25356970 PMID:25498144 PMID:25525159 PMID:25558065 PMID:25741868 PMID:26467025 PMID:26640698 PMID:26757139 PMID:27106809 PMID:27142713 PMID:27848944 PMID:28492532 PMID:29159460 PMID:29255295 PMID:29482223 PMID:29915382 PMID:30548255 PMID:30637285 PMID:30850373 PMID:30968303 PMID:31589614 PMID:31621627 PMID:31890231 PMID:32337771 PMID:32637629 PMID:32685350 PMID:32743982 PMID:32771712 PMID:32830305 PMID:32961396 PMID:33098801 PMID:33622667 PMID:33949708 PMID:34445196 PMID:34663476 PMID:34712575 PMID:9536098


    • Go Back to source page   Continue to Ontology report