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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Lgi1 and familial temporal lobe epilepsy 1 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 LGI1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 RGD objects have been annotated to familial temporal lobe epilepsy 1  (DOID:0060748)
  • 16 papers in RGD have been used to annotate Lgi1


    • An association has been curated linking Lgi1 and familial temporal lobe epilepsy 1 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 LGI1 (Homo sapiens) [(EXP) inferred from experiment]
  • 10 RGD objects have been annotated to familial temporal lobe epilepsy 1  (DOID:0060748)
  • 16 papers in RGD have been used to annotate Lgi1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Lgi1 and familial temporal lobe epilepsy 1 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 Lgi1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 10 RGD objects have been annotated to familial temporal lobe epilepsy 1  (DOID:0060748)
  • 16 papers in RGD have been used to annotate Lgi1
  • Curation Notes: OMIM:600512


    • An association has been curated linking Lgi1 and familial temporal lobe epilepsy 1 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 LGI1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 10 RGD objects have been annotated to familial temporal lobe epilepsy 1  (DOID:0060748)
  • 16 papers in RGD have been used to annotate Lgi1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant epilepsy with auditory features | ClinVar Annotator: match by term: Epilepsy, familial temporal lobe, 1 | ClinVar Annotator: match by term: LGI1-related condition
  • Original References(s): PMID:11810107 PMID:11978770 PMID:12205652 PMID:12601709 PMID:12771268 PMID:14510822 PMID:15079010 PMID:15079011 PMID:15349881 PMID:15660777 PMID:15857855 PMID:16199547 PMID:17067999 PMID:17296837 PMID:17562837 PMID:17576681 PMID:18414213 PMID:18625862 PMID:18711109 PMID:19780791 PMID:20659151 PMID:20863412 PMID:21444903 PMID:21504429 PMID:22496201 PMID:24206907 PMID:25485908 PMID:25741868 PMID:26467025 PMID:26773249 PMID:26993267 PMID:27760137 PMID:28492532 PMID:29133209 PMID:29670100 PMID:29924869 PMID:30284771 PMID:32086284 PMID:9536098


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