Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease UNIPROT Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease CLINVAR Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein. 15034582 2004
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease UNIPROT Mutant valosin-containing protein causes a novel type of frontotemporal dementia. 15732117 2005
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease UNIPROT Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene. 16247064 2005
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene. 16247064 2005
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease UNIPROT Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. 16321991 2006
Entrez Id: 84896
Gene Symbol: ATAD1
ATAD1 		0.020 Biomarker disease BEFREE The C-terminal 19-ku fragments of MSP1 (MSP-1(19)) of Plasmodium yoelii 265-BY was expressed in L. lactis and the recombinant L. lactis was administered orally to BALB/c and C57BL/6 mice. 16437602 2005
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Valosin-containing protein gene mutations: clinical and neuropathologic features. 16790606 2006
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Pathological consequences of VCP mutations on human striated muscle. 16984901 2007
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation. 17889967 2009
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease UNIPROT Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. 17935506 2007
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies. 19225410 2009
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death. 19237541 2009
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. 19704082 2009
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease CLINVAR Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. 19704082 2009
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease UNIPROT VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD. 20104022 2010
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease UNIPROT Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings. 20335036 2010
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 GeneticVariation disease UNIPROT A novel ATP-dependent conformation in p97 N-D1 fragment revealed by crystal structures of disease-related mutants. 20512113 2010
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 Biomarker disease GENOMICS_ENGLAND Exome sequencing reveals VCP mutations as a cause of familial ALS. 21145000 2010
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Exome sequencing reveals VCP mutations as a cause of familial ALS. 21145000 2010
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Valosin-containing protein gene mutations: cellular phenotypes relevant to neurodegeneration. 21249466 2011
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 Biomarker disease GENOMICS_ENGLAND Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish family. 21684747 2011
Entrez Id: 7415
Gene Symbol: VCP
VCP 		0.610 CausalMutation disease CLINVAR Valosin-containing protein mutation and Parkinson's disease. 21816654 2012