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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Reep1 and hereditary spastic paraplegia 31 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 REEP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 16 RGD objects have been annotated to hereditary spastic paraplegia 31  (DOID:0110782)
  • 4 papers in RGD have been used to annotate Reep1


    • An association has been curated linking Reep1 and hereditary spastic paraplegia 31 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 Reep1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 16 RGD objects have been annotated to hereditary spastic paraplegia 31  (DOID:0110782)
  • 4 papers in RGD have been used to annotate Reep1
  • Curation Notes: OMIM:610250


    • An association has been curated linking Reep1 and hereditary spastic paraplegia 31 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 REEP1 (Homo sapiens) [(EXP) inferred from experiment]
  • 16 RGD objects have been annotated to hereditary spastic paraplegia 31  (DOID:0110782)
  • 4 papers in RGD have been used to annotate Reep1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Reep1 and hereditary spastic paraplegia 31 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 REEP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 16 RGD objects have been annotated to hereditary spastic paraplegia 31  (DOID:0110782)
  • 4 papers in RGD have been used to annotate Reep1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 31 | ClinVar Annotator: match by term: Spastic paraplegia 31, autosomal dominant
  • Original References(s): PMID:16199547 PMID:16826527 PMID:17576681 PMID:18321925 PMID:18644145 PMID:19034539 PMID:19072839 PMID:20718791 PMID:21618648 PMID:22062632 PMID:22703882 PMID:23108492 PMID:23812641 PMID:24051375 PMID:24098485 PMID:24451228 PMID:24478229 PMID:24604904 PMID:24986827 PMID:25025039 PMID:25525159 PMID:25640679 PMID:25741868 PMID:26201691 PMID:26392352 PMID:26467025 PMID:26671083 PMID:27066569 PMID:28362824 PMID:28492532 PMID:29124833 PMID:29629531 PMID:30373780 PMID:30564185 PMID:30637453 PMID:31872057 PMID:32501971 PMID:32581362 PMID:32655478 PMID:9536098


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