EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.6.4.7 | Acquired Immunodeficiency Syndrome |
16321991 |
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation. |
causal interaction
unassigned |
4
0 |
| 3.6.4.7 | Adenocarcinoma |
14761919 |
Increased expression of valosin-containing protein (p97) is associated with lymph node metastasis and prognosis of pancreatic ductal adenocarcinoma. |
causal interaction
diagnostic usage
unassigned |
4
2
0 |
| 3.6.4.7 | Adrenoleukodystrophy |
11216907 |
Organelle disease: peroxisomal disorders. |
causal interaction
unassigned |
3
0 |
| 3.6.4.7 | Alzheimer Disease |
17622780 |
Identification of a novel valosin-containing protein polymorphism in late-onset Alzheimer's disease. |
causal interaction
unassigned |
4
0 |
| 3.6.4.7 | Amyotrophic Lateral Sclerosis |
20496755 |
[The molecular pathology of frontotemporal lobar degeneration] |
causal interaction
unassigned |
1
0 |
| 3.6.4.7 | Amyotrophic Lateral Sclerosis |
21145000 |
Exome sequencing reveals VCP mutations as a cause of familial ALS. |
ongoing research
unassigned |
3
0 |
| 3.6.4.7 | Amyotrophic Lateral Sclerosis |
22040362 |
Characterization of the Asian myopathy patients with VCP mutations. |
causal interaction
unassigned |
3
0 |
| 3.6.4.7 | Amyotrophic Lateral Sclerosis |
22078486 |
VCP mutations in familial and sporadic amyotrophic lateral sclerosis. |
unassigned |
0 |
| 3.6.4.7 | Amyotrophic Lateral Sclerosis |
22137929 |
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis. |
causal interaction
unassigned |
4
0 |
| 3.6.4.7 | Amyotrophic Lateral Sclerosis |
22210628 |
Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy. |
causal interaction
unassigned |
1
0 |
