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GENE - TERM ANNOTATION REPORT

75 Annotations Found.

An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:40904506 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:127316388 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:40906320 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15129024 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15099623 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:13540469 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753883 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151731597 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:127328007 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753903 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753872 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:40906322 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:13622830 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753970 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753823 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753985 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:23176824


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12738989 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:23176824 PMID:25590979 PMID:25741868 PMID:26542466 PMID:28492532 PMID:33847017


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753957 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15127563 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753926 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:40904509 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15120531 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:127321547 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151731611 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:13817995 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12889131 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753847 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753964 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12882227 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753864 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:10768208 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:38456355 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:27406698 PMID:28492532 PMID:30681437 PMID:32209221 PMID:33847017


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12841774 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12840226 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753876 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12891168 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753919 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753841 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12886671 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12891808 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:11347604 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753935 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151731606 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151885080 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:23176824 PMID:25590979 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15137909 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753953 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12836174 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:11346829 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:13477525 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:14701772 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15120031 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:14717171 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15123410 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:13532609 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12891562 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15131682 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753976 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:13497554 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:13537588 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151757282 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753896 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:15143862 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12842765 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:27406698 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753946 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:11348285 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:10767481 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:12845876 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:156451287 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753855 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:150531006 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:38490883 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32657593


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:150431317 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:13622860 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29908077


  • An association has been curated linking TECPR2 and hereditary spastic paraplegia 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:151753830 (Homo sapiens)
  • 567 RGD objects have been annotated to hereditary spastic paraplegia  (DOID:2476)
  • 4 papers in RGD have been used to annotate TECPR2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary spastic paraplegia
  • Original References(s): PMID:25741868 PMID:28492532


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