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GENE - TERM ANNOTATION REPORT

31 Annotations Found.

An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:28871098 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:26884178


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8600263 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:10026181 PMID:11841555 PMID:492197 PMID:698095


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8687457 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:24728327 PMID:25741868


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8600265 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:12060391


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8565688 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:11219864 PMID:11841555


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8565687 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:11841555 PMID:492197 PMID:698095


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8600259 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:10026181 PMID:17466625 PMID:7951246 PMID:9096355


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8686548 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:22821389 PMID:24728327 PMID:25741868 PMID:27104957 PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8687471 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:24728327 PMID:25741868 PMID:28492532 PMID:29891518


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8687455 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:15682379 PMID:16550608 PMID:24728327 PMID:25741868 PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:11620866 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30086788 PMID:30306255


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8600264 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:12060391 PMID:23255472 PMID:23370536 PMID:25795128 PMID:26149386 PMID:32522879


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:10401405 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:15082767 PMID:24033266 PMID:25714468 PMID:28654958 PMID:33219753


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:28871102 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:16550608 PMID:25741868


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:42722888 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29641532 PMID:30306255


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:11609956 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:26580448 PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:151727600 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:24354460 PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G in Homo sapiens.        

  • 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 Ercc5 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: OMIM:278780


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens) & RGD:11601087|RGD:11617234|RGD:11618130|RGD:11620713|RGD:151355780|RGD:155268093|RGD:28867719|RGD:28868544|RGD:28871266|RGD:28910959|RGD:28911086|RGD:401917943 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:25741868


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:405281857 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:25741915


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8687449|RGD:8687452|RGD:8687458|RGD:8687464|RGD:8687465|RGD:8687478|RGD:8687479 (Homo sapiens) & RGD:8687449|RGD:8687452|RGD:8687458|RGD:8687464|RGD:8687465|RGD:8687478|RGD:8687479 (Homo sapiens) & RGD:8687449|RGD:8687452|RGD:8687458|RGD:8687464|RGD:8687465|RGD:8687478|RGD:8687479 (Homo sapiens) & RGD:8687449|RGD:8687452|RGD:8687458|RGD:8687464|RGD:8687465|RGD:8687478|RGD:8687479 (Homo sapiens) & RGD:8687449|RGD:8687452|RGD:8687458|RGD:8687464|RGD:8687465|RGD:8687478|RGD:8687479 (Homo sapiens) & RGD:8687449|RGD:8687452|RGD:8687458|RGD:8687464|RGD:8687465|RGD:8687478|RGD:8687479 (Homo sapiens) & RGD:8687449|RGD:8687452|RGD:8687458|RGD:8687464|RGD:8687465|RGD:8687478|RGD:8687479 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:24728327 PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens) & RGD:11546872|RGD:11550452|RGD:11550689|RGD:11551460|RGD:11603984|RGD:11613010|RGD:11615882|RGD:11618767|RGD:11618899|RGD:11619676|RGD:11621206|RGD:11622845|RGD:11624569|RGD:11626127|RGD:13534163|RGD:150553999|RGD:15100301|RGD:21072555|RGD:8659519 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens) & RGD:11599232|RGD:11614082|RGD:11619294|RGD:11622320|RGD:11622526|RGD:11660457|RGD:13534156|RGD:15109698|RGD:15132865|RGD:15162404|RGD:15162409|RGD:28910961 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens) & RGD:8659520|RGD:8659521|RGD:8659522|RGD:8687446|RGD:8687447|RGD:8687460|RGD:8687461|RGD:8687466|RGD:8687467|RGD:8687468|RGD:8687475|RGD:8687481 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:24728327 PMID:25741868 PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens) & RGD:11600285|RGD:11600979|RGD:11604269|RGD:11606641|RGD:11607377|RGD:11610216|RGD:11610890|RGD:11612163|RGD:11615134|RGD:11618584|RGD:11620340|RGD:11621004|RGD:11622641|RGD:11623263|RGD:11623793|RGD:11624053|RGD:11624940|RGD:11625923|RGD:11626032|RGD:11644848|RGD:11653495|RGD:11662258|RGD:13534160|RGD:14693051|RGD:21072556|RGD:28867724|RGD:28868276|RGD:28868420|RGD:28868547|RGD:28868551|RGD:28868655|RGD:28868659|RGD:28870777|RGD:28870779|RGD:28870924|RGD:28870928|RGD:28870932|RGD:28871095|RGD:28871263|RGD:28910958|RGD:28910962|RGD:28911006|RGD:28911047|RGD:28911048|RGD:28911087|RGD:28911450|RGD:28911451|RGD:401828983|RGD:401828985 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8565689 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:11841555 PMID:23370536 PMID:24700531 PMID:28492532


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8687462|RGD:8687469 (Homo sapiens) & RGD:8687462|RGD:8687469 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:24728327


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8600258 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:23370536 PMID:24700531 PMID:28492532 PMID:30919937 PMID:7951246


  • An association has been curated linking ERCC5 and xeroderma pigmentosum group G 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:8604642|RGD:8604643 (Homo sapiens) & RGD:8604642|RGD:8604643 (Homo sapiens)
  • 3 RGD objects have been annotated to xeroderma pigmentosum group G  (DOID:0110849)
  • 20 papers in RGD have been used to annotate ERCC5
  • Curation Notes: ClinVar Annotator: match by term: Xeroderma pigmentosum, group G
  • Original References(s): PMID:23255472


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