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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Lrat and Leber congenital amaurosis 14 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 LRAT (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Leber congenital amaurosis 14  (DOID:0110188)
  • 19 papers in RGD have been used to annotate Lrat


    • An association has been curated linking Lrat and Leber congenital amaurosis 14 in Mus musculus.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • 2 RGD objects have been annotated to Leber congenital amaurosis 14  (DOID:0110188)
  • 19 papers in RGD have been used to annotate Lrat
  • Curation Notes: OMIM:613341


    • An association has been curated linking Lrat and Leber congenital amaurosis 14 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 LRAT (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to Leber congenital amaurosis 14  (DOID:0110188)
  • 19 papers in RGD have been used to annotate Lrat
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Lrat and Leber congenital amaurosis 14 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 LRAT (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Leber congenital amaurosis 14  (DOID:0110188)
  • 19 papers in RGD have been used to annotate Lrat
  • Curation Notes: ClinVar Annotator: match by term: LRAT-related condition | ClinVar Annotator: match by term: Leber congenital amaurosis 14 | ClinVar Annotator: match by term: RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED | ClinVar Annotator: match by term: RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED
  • Original References(s): PMID:11381255 PMID:17011878 PMID:18055821 PMID:22025579 PMID:22559933 PMID:22570351 PMID:24265693 PMID:25741868 PMID:26656277 PMID:27854360 PMID:28492532 PMID:29186038 PMID:30054919 PMID:32865313


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