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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking LRRC56 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:11348575 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate LRRC56
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking LRRC56 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:9689988 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate LRRC56
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:22683711 PMID:24033266 PMID:24259709 PMID:25741868 PMID:28492532 PMID:8605880


    • An association has been curated linking LRRC56 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:8563224 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate LRRC56
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:11150980 PMID:16155195 PMID:16170316 PMID:16329078 PMID:16372351 PMID:16443854 PMID:16835863 PMID:16881968 PMID:16969868 PMID:17054105 PMID:17412879 PMID:18039947 PMID:18247425 PMID:18978862 PMID:19206176 PMID:19371735 PMID:19669404 PMID:20660566 PMID:20979192 PMID:21834037 PMID:21850009 PMID:22087699 PMID:22317973 PMID:22495892 PMID:22683711 PMID:23751039 PMID:24033266 PMID:24129065 PMID:24224811 PMID:25741868 PMID:25815234 PMID:25914166 PMID:26467025 PMID:26619011 PMID:26778095 PMID:28139825 PMID:28492532 PMID:29493581 PMID:30055033 PMID:30138938 PMID:31560489 PMID:31564432 PMID:31775759 PMID:32371413 PMID:33372952 PMID:34008892


    • An association has been curated linking LRRC56 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:151780056 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate LRRC56
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LRRC56 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:8563222 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate LRRC56
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:16170316 PMID:17384584 PMID:17412879 PMID:19255327 PMID:19773371 PMID:22495892 PMID:22499344 PMID:23406027 PMID:24033266 PMID:25157968 PMID:25741868 PMID:2999610 PMID:3537694 PMID:6092966 PMID:6330729 PMID:7177195 PMID:8960317


    • An association has been curated linking LRRC56 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:8563225 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate LRRC56
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:16170316 PMID:16372351 PMID:16443854 PMID:16835863 PMID:17601930 PMID:17979197 PMID:18042262 PMID:20979192 PMID:21686750 PMID:21834037 PMID:21850009 PMID:22317973 PMID:22420426 PMID:23093928 PMID:23751039 PMID:24169525 PMID:24224811 PMID:24803665 PMID:25741868 PMID:26619011 PMID:27195699 PMID:27589201 PMID:28027064 PMID:28492532


    • An association has been curated linking LRRC56 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:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens) & RGD:13527898|RGD:151721672|RGD:151745282|RGD:151758734|RGD:151760798|RGD:151788522|RGD:151819032|RGD:151857785|RGD:151880998|RGD:151883749|RGD:151888458|RGD:156210760|RGD:156227707|RGD:156299962|RGD:156394795 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate LRRC56
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking LRRC56 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:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens) & RGD:155925152|RGD:155953762|RGD:156148990|RGD:156296557|RGD:156297228|RGD:156335095|RGD:156359591|RGD:156389075|RGD:156395337|RGD:156399806|RGD:329363664|RGD:329373085|RGD:329379704|RGD:329389894|RGD:329399201|RGD:401725478|RGD:401743248|RGD:401746073|RGD:401758959|RGD:401760701|RGD:401779183|RGD:401782671|RGD:401856196|RGD:401881508|RGD:401887342 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate LRRC56
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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