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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking DLG3 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:10408274 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate DLG3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking DLG3 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:11049696 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate DLG3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28554332


    • An association has been curated linking DLG3 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:10404035|RGD:126742022|RGD:13215295|RGD:13829720|RGD:13829746|RGD:151349709 (Homo sapiens) & RGD:10404035|RGD:126742022|RGD:13215295|RGD:13829720|RGD:13829746|RGD:151349709 (Homo sapiens) & RGD:10404035|RGD:126742022|RGD:13215295|RGD:13829720|RGD:13829746|RGD:151349709 (Homo sapiens) & RGD:10404035|RGD:126742022|RGD:13215295|RGD:13829720|RGD:13829746|RGD:151349709 (Homo sapiens) & RGD:10404035|RGD:126742022|RGD:13215295|RGD:13829720|RGD:13829746|RGD:151349709 (Homo sapiens) & RGD:10404035|RGD:126742022|RGD:13215295|RGD:13829720|RGD:13829746|RGD:151349709 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate DLG3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


    • An association has been curated linking DLG3 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:10048546|RGD:10404498|RGD:13828812|RGD:15161366|RGD:8642931 (Homo sapiens) & RGD:10048546|RGD:10404498|RGD:13828812|RGD:15161366|RGD:8642931 (Homo sapiens) & RGD:10048546|RGD:10404498|RGD:13828812|RGD:15161366|RGD:8642931 (Homo sapiens) & RGD:10048546|RGD:10404498|RGD:13828812|RGD:15161366|RGD:8642931 (Homo sapiens) & RGD:10048546|RGD:10404498|RGD:13828812|RGD:15161366|RGD:8642931 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate DLG3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking DLG3 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:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens) & RGD:13532280|RGD:13532628|RGD:13828554|RGD:13829204|RGD:150551116|RGD:155683418|RGD:155685817|RGD:155698651|RGD:155705812|RGD:155721149|RGD:155722937|RGD:155734413|RGD:155910029|RGD:156035688|RGD:156041279|RGD:156061211|RGD:156079147|RGD:156287045|RGD:156344648|RGD:156386968|RGD:329388857|RGD:329390871|RGD:401761231|RGD:40886548|RGD:40887161|RGD:40887377 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 7 papers in RGD have been used to annotate DLG3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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