EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.3.1.42 | Adrenoleukodystrophy |
2464339 |
Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblasts. |
ongoing research
unassigned |
2
0 |
| 2.3.1.42 | Carcinoma, Hepatocellular |
2169517 |
Lipid composition of hepatitis B virus surface antigen particles and the particle-producing human hepatoma cell lines. |
diagnostic usage
unassigned |
1
0 |
| 2.3.1.42 | Carcinoma, Hepatocellular |
31974474 |
Stabilization of FASN by ACAT1-mediated GNPAT acetylation promotes lipid metabolism and hepatocarcinogenesis. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
1
3
0 |
| 2.3.1.42 | Chondrodysplasia Punctata |
7914249 |
Chondrodysplasia punctata with a mild clinical course. |
causal interaction
unassigned |
1
0 |
| 2.3.1.42 | Chondrodysplasia Punctata |
8832947 |
X-linked dominant chondrodysplasia punctata with decreased dihydroxyacetone phosphate acyltransferase activity. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
2
0 |
| 2.3.1.42 | Chondrodysplasia Punctata |
9165515 |
Abnormal myelination in peroxisomal isolated dihydroxyacetonephosphate acyltransferase deficiency. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.3.1.42 | Chondrodysplasia Punctata, Rhizomelic |
2183242 |
Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes. |
causal interaction
unassigned |
1
0 |
| 2.3.1.42 | Chondrodysplasia Punctata, Rhizomelic |
2464339 |
Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblasts. |
ongoing research
unassigned |
2
0 |
| 2.3.1.42 | Chondrodysplasia Punctata, Rhizomelic |
7530787 |
Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delay. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.3.1.42 | Chondrodysplasia Punctata, Rhizomelic |
7914249 |
Chondrodysplasia punctata with a mild clinical course. |
causal interaction
unassigned |
1
0 |
