EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.3.1.199 | Acanthosis Nigricans |
30487246 |
De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy. |
causal interaction unassigned |
2 0 |
2.3.1.199 | Adrenoleukodystrophy |
20166112 |
The role of ELOVL1 in very long-chain fatty acid homeostasis and X-linked adrenoleukodystrophy. |
causal interaction ongoing research therapeutic application unassigned |
4 1 4 0 |
2.3.1.199 | Adrenoleukodystrophy |
22911730 |
Bezafibrate for x-linked adrenoleukodystrophy. |
causal interaction therapeutic application unassigned |
2 4 0 |
2.3.1.199 | Adrenoleukodystrophy |
25499606 |
Enzymatic characterization of ELOVL1, a key enzyme in very long-chain fatty acid synthesis. |
causal interaction diagnostic usage ongoing research therapeutic application |
4 3 4 1 |
2.3.1.199 | Breast Neoplasms |
21415164 |
Novel theranostic opportunities offered by characterization of altered membrane lipid metabolism in breast cancer progression. |
unassigned |
0 |
2.3.1.199 | Breast Neoplasms |
27788154 |
Estrogen Enhances the Expression of the Polyunsaturated Fatty Acid Elongase Elovl2 via ER? in Breast Cancer Cells. |
ongoing research unassigned |
3 0 |
2.3.1.199 | Corneal Opacity |
29401594 |
Very long-chain tear film lipids produced by fatty acid elongase ELOVL1 prevent dry eye disease in mice. |
unassigned |
0 |
2.3.1.199 | Deafness |
30487246 |
De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy. |
causal interaction unassigned |
2 0 |
2.3.1.199 | Deafness |
32123819 |
Reduced chain length in myelin sphingolipids and poorer motor coordination in mice deficient in the fatty acid elongase Elovl1. |
causal interaction ongoing research therapeutic application unassigned |
3 4 1 0 |
2.3.1.199 | Demyelinating Diseases |
20035504 |
Dicer ablation in oligodendrocytes provokes neuronal impairment in mice. |
causal interaction therapeutic application unassigned |
3 1 0 |