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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking LOC129997861 and hereditary spastic paraplegia 48 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:156216383 (Homo sapiens)
  • 5 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 0 papers in RGD have been used to annotate LOC129997861
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 48
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking LOC129997861 and hereditary spastic paraplegia 48 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13808151 (Homo sapiens)
  • 5 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 0 papers in RGD have been used to annotate LOC129997861
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 48
  • Original References(s): PMID:25741868 PMID:26467025


    • An association has been curated linking LOC129997861 and hereditary spastic paraplegia 48 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11586874 (Homo sapiens)
  • 5 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 0 papers in RGD have been used to annotate LOC129997861
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 48
  • Original References(s): PMID:25741868


    • An association has been curated linking LOC129997861 and hereditary spastic paraplegia 48 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:151714032 (Homo sapiens)
  • 5 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 0 papers in RGD have been used to annotate LOC129997861
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 48
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LOC129997861 and hereditary spastic paraplegia 48 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:155941417|RGD:155997542|RGD:156259370|RGD:26888247 (Homo sapiens) & RGD:155941417|RGD:155997542|RGD:156259370|RGD:26888247 (Homo sapiens) & RGD:155941417|RGD:155997542|RGD:156259370|RGD:26888247 (Homo sapiens) & RGD:155941417|RGD:155997542|RGD:156259370|RGD:26888247 (Homo sapiens)
  • 5 RGD objects have been annotated to hereditary spastic paraplegia 48  (DOID:0110800)
  • 0 papers in RGD have been used to annotate LOC129997861
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia 48
  • Original References(s): PMID:28492532


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