EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.1.1.102 | Carcinogenesis |
15505035 |
Identification of target genes regulated by FOXC1 using nickel agarose-based chromatin enrichment. |
causal interaction
therapeutic application
unassigned |
2
1
0 |
| 1.1.1.102 | Ichthyosis |
34277909 |
Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation. |
causal interaction
unassigned |
2
0 |
| 1.1.1.102 | Leukemia |
34373586 |
3-Ketodihydrosphingosine reductase maintains ER homeostasis and unfolded protein response in leukemia. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
1
2
1
0 |
| 1.1.1.102 | Lymphoma, Follicular |
8417785 |
FVT-1, a novel human transcription unit affected by variant translocation t(2;18)(p11;q21) of follicular lymphoma. |
causal interaction
unassigned |
3
0 |
| 1.1.1.102 | Muscular Atrophy, Spinal |
17420465 |
A missense mutation in the 3-ketodihydrosphingosine reductase FVT1 as candidate causal mutation for bovine spinal muscular atrophy. |
causal interaction
unassigned |
3
0 |
| 1.1.1.102 | Neoplasms |
8417785 |
FVT-1, a novel human transcription unit affected by variant translocation t(2;18)(p11;q21) of follicular lymphoma. |
causal interaction
unassigned |
3
0 |
| 1.1.1.102 | Thrombocytopenia |
34277909 |
Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation. |
causal interaction
unassigned |
2
0 |
