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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking ALG13 and genetic disease 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:12880821 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate ALG13
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:24476948 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking ALG13 and genetic disease 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:8573557 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate ALG13
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:23033978 PMID:23934111 PMID:24781210 PMID:24896178 PMID:25732998 PMID:25741868 PMID:26138355 PMID:26482601 PMID:28492532 PMID:28778787 PMID:28887793 PMID:28940310 PMID:32238909 PMID:32681751 PMID:33734437


    • An association has been curated linking ALG13 and genetic disease 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:10401494 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate ALG13
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


    • An association has been curated linking ALG13 and genetic disease 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:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens) & RGD:11349733|RGD:126771353|RGD:127240230|RGD:12842448|RGD:12844812|RGD:12913455|RGD:13497730|RGD:13528605|RGD:13535137|RGD:13541548|RGD:13821629|RGD:13828958|RGD:13829927|RGD:13830173|RGD:14735514|RGD:15174306|RGD:151870359|RGD:152144923|RGD:155718518|RGD:155732825|RGD:156112521|RGD:38472063 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate ALG13
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking ALG13 and genetic disease 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:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens) & RGD:11348452|RGD:11641244|RGD:12833723|RGD:12834191|RGD:12839201|RGD:12839729|RGD:12843108|RGD:12844670|RGD:12845570|RGD:12847941|RGD:12889923|RGD:12900367|RGD:13500736|RGD:13535449|RGD:13540201|RGD:13622884|RGD:13829151|RGD:14738539|RGD:15125894 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate ALG13
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ALG13 and genetic disease 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:11345786|RGD:11349893|RGD:12833677|RGD:12835099|RGD:12845500 (Homo sapiens) & RGD:11345786|RGD:11349893|RGD:12833677|RGD:12835099|RGD:12845500 (Homo sapiens) & RGD:11345786|RGD:11349893|RGD:12833677|RGD:12835099|RGD:12845500 (Homo sapiens) & RGD:11345786|RGD:11349893|RGD:12833677|RGD:12835099|RGD:12845500 (Homo sapiens) & RGD:11345786|RGD:11349893|RGD:12833677|RGD:12835099|RGD:12845500 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate ALG13
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking ALG13 and genetic disease 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:12834599|RGD:13808103 (Homo sapiens) & RGD:12834599|RGD:13808103 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate ALG13
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:26467025 PMID:28492532


    • An association has been curated linking ALG13 and genetic disease 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:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens) & RGD:13828643|RGD:13829389|RGD:13829567|RGD:155720741|RGD:155747748|RGD:155991973|RGD:156011521|RGD:156058854|RGD:156358620|RGD:156383069|RGD:40887084|RGD:40887309 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate ALG13
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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