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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Spg21 and MAST syndrome 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 SPG21 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MAST syndrome  (DOID:0060245)
  • 11 papers in RGD have been used to annotate Spg21


    • An association has been curated linking Spg21 and MAST syndrome 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 Spg21 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MAST syndrome  (DOID:0060245)
  • 11 papers in RGD have been used to annotate Spg21
  • Curation Notes: OMIM:248900


    • An association has been curated linking Spg21 and MAST syndrome 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 SPG21 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to MAST syndrome  (DOID:0060245)
  • 11 papers in RGD have been used to annotate Spg21
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Spg21 and MAST syndrome 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 SPG21 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MAST syndrome  (DOID:0060245)
  • 11 papers in RGD have been used to annotate Spg21
  • Curation Notes: ClinVar Annotator: match by term: Mast syndrome | ClinVar Annotator: match by term: SPASTIC PARAPLEGIA 21, AUTOSOMAL RECESSIVE
  • Original References(s): PMID:14564668 PMID:16199547 PMID:17576681 PMID:24451228 PMID:25741868 PMID:25741909 PMID:26467025 PMID:28492532 PMID:28752238 PMID:35111129 PMID:6024251 PMID:9536098


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