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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking C1qtnf5 and late-onset retinal degeneration 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 C1QTNF5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to late-onset retinal degeneration  (DOID:0060869)
  • 6 papers in RGD have been used to annotate C1qtnf5


    • An association has been curated linking C1qtnf5 and late-onset retinal degeneration 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 C1qtnf5 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to late-onset retinal degeneration  (DOID:0060869)
  • 6 papers in RGD have been used to annotate C1qtnf5
  • Curation Notes: OMIM:605670


    • An association has been curated linking C1qtnf5 and late-onset retinal degeneration 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 C1QTNF5 (Homo sapiens) [(EXP) inferred from experiment]
  • 4 RGD objects have been annotated to late-onset retinal degeneration  (DOID:0060869)
  • 6 papers in RGD have been used to annotate C1qtnf5
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking C1qtnf5 and late-onset retinal degeneration 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 C1QTNF5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to late-onset retinal degeneration  (DOID:0060869)
  • 6 papers in RGD have been used to annotate C1qtnf5
  • Curation Notes: ClinVar Annotator: match by term: C1QTNF5-related condition | ClinVar Annotator: match by term: Late-onset retinal degeneration | ClinVar Annotator: match by term: RETINAL DEGENERATION, LATE-ONSET, AUTOSOMAL DOMINANT
  • Original References(s): PMID:12944416 PMID:18648522 PMID:19169412 PMID:22892318 PMID:23289492 PMID:24531000 PMID:25326637 PMID:25741868 PMID:28492532 PMID:28939808 PMID:29847639 PMID:32483926 PMID:3394928 PMID:33949280


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