EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.1.1.77 | Adenocarcinoma of Lung |
26997432 |
Chaperone protein L-isoaspartate (D-aspartyl) O-methyltransferase as a novel predictor of poor prognosis in lung adenocarcinoma. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
3
4
2
4 |
| 2.1.1.77 | Alzheimer Disease |
2002878 |
Protein L-isoaspartyl methyltransferase in postmortem brains of aged humans. |
causal interaction
unassigned |
1
0 |
| 2.1.1.77 | Anencephaly |
22647835 |
Maternal PCMT1 gene polymorphisms and the risk of neural tube defects in a Chinese population of Lvliang high-risk area. |
diagnostic usage
therapeutic application
unassigned |
2
1
0 |
| 2.1.1.77 | Ataxia |
14503922 |
Spectrum of centrosome autoantibodies in childhood varicella and post-varicella acute cerebellar ataxia. |
ongoing research
unassigned |
2
0 |
| 2.1.1.77 | Carcinoma |
33898446 |
LINC00511/miRNA-143-3p Modulates Apoptosis and Malignant Phenotype of Bladder Carcinoma Cells via PCMT1. |
diagnostic usage
ongoing research
unassigned |
3
3
0 |
| 2.1.1.77 | Carcinoma, Hepatocellular |
25119594 |
Hsa-miR-195 targets PCMT1 in hepatocellular carcinoma that increases tumor life span. |
causal interaction
unassigned |
3
0 |
| 2.1.1.77 | Ciliopathies |
21266464 |
Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 2.1.1.77 | Diabetes Mellitus, Type 1 |
19290383 |
Posttranslational Protein Modifications in Type 1 Diabetes - Genetic Studies with PCMT1, the Repair Enzyme Protein Isoaspartate Methyltransferase (PIMT) Encoding Gene. |
therapeutic application
unassigned |
1
0 |
| 2.1.1.77 | Epilepsy |
9482793 |
Deficiency in protein L-isoaspartyl methyltransferase results in a fatal progressive epilepsy. |
causal interaction
ongoing research
unassigned |
4
3
0 |
| 2.1.1.77 | Epilepsy |
12125075 |
Transgenic expression of the protein-L-isoaspartyl methyltransferase (PIMT) gene in the brain rescues mice from the fatal epilepsy of PIMT deficiency. |
causal interaction
ongoing research
unassigned |
1
2
0 |
