EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.1.3.56 | Alzheimer Disease |
27750211 |
INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis. |
causal interaction |
4 |
| 3.1.3.56 | Alzheimer Disease |
27750211 |
INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis. |
diagnostic usage |
3 |
| 3.1.3.56 | Alzheimer Disease |
27750211 |
INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis. |
ongoing research |
1 |
| 3.1.3.56 | Alzheimer Disease |
27750211 |
INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis. |
unassigned |
0 |
| 3.1.3.56 | Astrocytoma |
24358143 |
Identification of novel genetic alterations in samples of malignant glioma patients. |
ongoing research |
2 |
| 3.1.3.56 | Astrocytoma |
24358143 |
Identification of novel genetic alterations in samples of malignant glioma patients. |
unassigned |
0 |
| 3.1.3.56 | Ataxia |
26051944 |
Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice. |
causal interaction |
2 |
| 3.1.3.56 | Ataxia |
33792664 |
INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH. |
causal interaction |
4 |
| 3.1.3.56 | Ataxia |
26051944 |
Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice. |
unassigned |
0 |
| 3.1.3.56 | Ataxia |
33792664 |
INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH. |
unassigned |
0 |
