EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    6.2.1.1 | - |
21841779 |
Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria. |
causal interaction
unassigned |
4
0 |
| 6.2.1.1 | acetate-coa ligase deficiency |
30228117 |
ACSS2 promotes systemic fat storage and utilization through selective regulation of genes involved in lipid metabolism. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
3
4
0 |
| 6.2.1.1 | Acquired Immunodeficiency Syndrome |
20877624 |
Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression. |
causal interaction
unassigned |
1
0 |
| 6.2.1.1 | Acquired Immunodeficiency Syndrome |
29457784 |
HIV latency is reversed by ACSS2-driven histone crotonylation. |
causal interaction
unassigned |
2
0 |
| 6.2.1.1 | Adrenoleukodystrophy |
2117919 |
Metabolism of saturated and polyunsaturated very-long-chain fatty acids in fibroblasts from patients with defects in peroxisomal beta-oxidation. |
unassigned |
0 |
| 6.2.1.1 | Adrenoleukodystrophy |
11112418 |
Novel acyl-CoA synthetase in adrenoleukodystrophy target tissues. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 6.2.1.1 | Adrenoleukodystrophy |
11330068 |
Disruption of a yeast very-long-chain acyl-CoA synthetase gene simulates the cellular phenotype of X-linked adrenoleukodystrophy. |
causal interaction
unassigned |
2
0 |
| 6.2.1.1 | Adrenoleukodystrophy |
14516277 |
Murine bubblegum orthologue is a microsomal very long-chain acyl-CoA synthetase. |
causal interaction
unassigned |
3
0 |
| 6.2.1.1 | Adrenoleukodystrophy |
16371355 |
The second member of the human and murine bubblegum family is a testis- and brainstem-specific acyl-CoA synthetase. |
causal interaction
unassigned |
2
0 |
| 6.2.1.1 | Arachnoiditis |
26732971 |
Time-Spatial Labeling Inversion Pulse Magnetic Resonance Imaging of Cystic Lesions of the Spinal Cord. |
causal interaction
therapeutic application
unassigned |
2
1
0 |
