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GENE - TERM ANNOTATION REPORT

23 Annotations Found.

An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:8597937 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:8597938 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:16321991


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:8597936 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:16790606 PMID:16984901 PMID:17763460 PMID:19237541 PMID:19364651 PMID:21320982 PMID:22909335 PMID:23029473 PMID:23056506 PMID:25388089 PMID:25741868 PMID:26105173 PMID:27768726 PMID:28360103 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11546177 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:16790606 PMID:22137929 PMID:25741868 PMID:26467025 PMID:28130640 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11578900 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:25741868 PMID:26467025


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:8597940 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:19237541 PMID:21145000 PMID:21984748 PMID:22270372 PMID:22900631 PMID:23333620 PMID:23498975 PMID:24196964 PMID:25741868 PMID:26105173 PMID:26467025 PMID:27226613 PMID:27708273 PMID:28360103 PMID:28492532 PMID:28692196 PMID:30279455


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11643254 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: MULTISYSTEM PROTEINOPATHY 1
  • Original References(s): PMID:21387114 PMID:21920633 PMID:25617006 PMID:25741868 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:15135819 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:26467025 PMID:27790088 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11639469 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:22078486 PMID:25618255 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:8597939 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:17763460 PMID:19364651 PMID:19506019 PMID:20604808 PMID:25741868 PMID:26549226 PMID:28492532 PMID:28692196 PMID:7182974


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:8597935 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:16321991 PMID:16984901 PMID:17329348 PMID:18341608 PMID:19237541 PMID:20008565 PMID:20104022 PMID:20512113 PMID:20604808 PMID:20957154 PMID:21145000 PMID:21822278 PMID:22270372 PMID:22686199 PMID:22898872 PMID:23029473 PMID:23169451 PMID:23498975 PMID:24196964 PMID:25125609 PMID:25388089 PMID:25741868 PMID:25775548 PMID:26467025 PMID:28492532 PMID:30293881 PMID:31687228


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:13804184 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30005904


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:10448452 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:19704082 PMID:27538664 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:10406111 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:16790606 PMID:17763460 PMID:19364651 PMID:25326637 PMID:26105173 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:10050434|RGD:11603429|RGD:14731649|RGD:28876066|RGD:28883532|RGD:28883546 (Homo sapiens) & RGD:10050434|RGD:11603429|RGD:14731649|RGD:28876066|RGD:28883532|RGD:28883546 (Homo sapiens) & RGD:10050434|RGD:11603429|RGD:14731649|RGD:28876066|RGD:28883532|RGD:28883546 (Homo sapiens) & RGD:10050434|RGD:11603429|RGD:14731649|RGD:28876066|RGD:28883532|RGD:28883546 (Homo sapiens) & RGD:10050434|RGD:11603429|RGD:14731649|RGD:28876066|RGD:28883532|RGD:28883546 (Homo sapiens) & RGD:10050434|RGD:11603429|RGD:14731649|RGD:28876066|RGD:28883532|RGD:28883546 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1 | ClinVar Annotator: match by term: MULTISYSTEM PROTEINOPATHY 1
  • Original References(s): PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11544847|RGD:11599280|RGD:28876472|RGD:28883540 (Homo sapiens) & RGD:11544847|RGD:11599280|RGD:28876472|RGD:28883540 (Homo sapiens) & RGD:11544847|RGD:11599280|RGD:28876472|RGD:28883540 (Homo sapiens) & RGD:11544847|RGD:11599280|RGD:28876472|RGD:28883540 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:8597941 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:16247064 PMID:19225410 PMID:19704082 PMID:22078486 PMID:22270372 PMID:24829604 PMID:25492614 PMID:25741868 PMID:26467025 PMID:26555887 PMID:27226613 PMID:28492532 PMID:28542158 PMID:29770363 PMID:30279455 PMID:31848255 PMID:31862442 PMID:32317127 PMID:32528171 PMID:34573259


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11578384 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:15034582 PMID:18845250 PMID:20604808 PMID:22270372 PMID:22909335 PMID:23333620 PMID:25617006 PMID:25741868 PMID:28492532 PMID:33144514


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11548452|RGD:11551995|RGD:38462114|RGD:38597833|RGD:401854273 (Homo sapiens) & RGD:11548452|RGD:11551995|RGD:38462114|RGD:38597833|RGD:401854273 (Homo sapiens) & RGD:11548452|RGD:11551995|RGD:38462114|RGD:38597833|RGD:401854273 (Homo sapiens) & RGD:11548452|RGD:11551995|RGD:38462114|RGD:38597833|RGD:401854273 (Homo sapiens) & RGD:11548452|RGD:11551995|RGD:38462114|RGD:38597833|RGD:401854273 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:25741868


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:10047969|RGD:11602508|RGD:11602759|RGD:13470598|RGD:28881379 (Homo sapiens) & RGD:10047969|RGD:11602508|RGD:11602759|RGD:13470598|RGD:28881379 (Homo sapiens) & RGD:10047969|RGD:11602508|RGD:11602759|RGD:13470598|RGD:28881379 (Homo sapiens) & RGD:10047969|RGD:11602508|RGD:11602759|RGD:13470598|RGD:28881379 (Homo sapiens) & RGD:10047969|RGD:11602508|RGD:11602759|RGD:13470598|RGD:28881379 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:26467025 PMID:28492532


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens) & RGD:11599930|RGD:11600054|RGD:11601083|RGD:11601818|RGD:11603345|RGD:11603816|RGD:11605101|RGD:11606388|RGD:11607424|RGD:11644555|RGD:11646696|RGD:11647267|RGD:11648561|RGD:11654150|RGD:11656370|RGD:11658814|RGD:11659737|RGD:28875738|RGD:28875741|RGD:28875882|RGD:28880910|RGD:28881129|RGD:28881136|RGD:28881375|RGD:28883045|RGD:28883525|RGD:28885719|RGD:28885727|RGD:28885946|RGD:28886172 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1 | ClinVar Annotator: match by term: MULTISYSTEM PROTEINOPATHY 1


    • An association has been curated linking VCP and inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 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:11545296|RGD:11552395 (Homo sapiens) & RGD:11545296|RGD:11552395 (Homo sapiens)
  • 1 RGD objects have been annotated to inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1  (DOID:0111385)
  • 11 papers in RGD have been used to annotate VCP
  • Curation Notes: ClinVar Annotator: match by term: Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


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