HCSGD entry for DLAT
1. General information
Official gene symbol | DLAT |
---|---|
Entrez ID | 1737 |
Gene full name | dihydrolipoamide S-acetyltransferase |
Other gene symbols | DLTA PDC-E2 PDCE2 |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

This gene isn't in Literature mining network.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0004742 | Dihydrolipoyllysine-residue acetyltransferase activity | IEA NAS | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005759 | Mitochondrial matrix | TAS | cellular_component |
GO:0005967 | Mitochondrial pyruvate dehydrogenase complex | NAS | cellular_component |
GO:0006006 | Glucose metabolic process | IEA | biological_process |
GO:0006090 | Pyruvate metabolic process | IEA TAS | biological_process |
GO:0006099 | Tricarboxylic acid cycle | IEA | biological_process |
GO:0010510 | Regulation of acetyl-CoA biosynthetic process from pyruvate | TAS | biological_process |
GO:0044237 | Cellular metabolic process | TAS | biological_process |
GO:0044281 | Small molecule metabolic process | TAS | biological_process |
GO:0045254 | Pyruvate dehydrogenase complex | IEA | cellular_component |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.6262170054 | 0.2896803997 | 0.9999902473 | 1.0000000000 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Up | 0.0889718330 |
GSE13712_SHEAR | Up | 0.1560344339 |
GSE13712_STATIC | Up | 0.1109985714 |
GSE19018 | Down | -0.3687556524 |
GSE19899_A1 | Up | 0.1106375160 |
GSE19899_A2 | Up | 0.1676900443 |
PubMed_21979375_A1 | Up | 0.3745380488 |
PubMed_21979375_A2 | Down | -0.0337298628 |
GSE35957 | Down | -0.2145368989 |
GSE36640 | Down | -0.1355278270 |
GSE54402 | Up | 0.3037785660 |
GSE9593 | Down | -0.4202960076 |
GSE43922 | Up | 0.1964042660 |
GSE24585 | Down | -0.3754670483 |
GSE37065 | Down | -0.0197393488 |
GSE28863_A1 | Down | -0.1753782535 |
GSE28863_A2 | Up | 0.1795603517 |
GSE28863_A3 | Down | -0.5943146574 |
GSE28863_A4 | Up | 0.1703058563 |
GSE48662 | Down | -0.3759374832 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Name | Drug | Accession number |
---|---|---|
NADH | DB00157 | NUTR00041 | DB01907 | EXPT02287 | DB03527 |
Radicicol | DB03758 | EXPT02763 |
Dihydrolipoic Acid | DB03760 | EXPT02769 |
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-let-7b-5p | MIMAT0000063 | MIRT032242 | Proteomics | Functional MTI (Weak) | 18668040 |
hsa-miR-615-3p | MIMAT0003283 | MIRT040451 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-10b-5p | MIMAT0000254 | MIRT047485 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
No target information from mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
26201620 | Biliary specificity in PBC is most likely driven by the uniqueness of cholangiocyte apoptosis in which the PDC-E2 autoantigen undergoes differential glutathiolation |
23231002 | METHODS: We examined immunohistochemically the expression of pyruvate dehydrogenase complex-E2 component (PDC-E2) and cytochrome c oxidase, subunit I (CCO), in livers taken from patients with PBC (n = 42) and control livers (n = 76) |
23231002 | RESULTS: Intense granular expression of PDC-E2 and CCO was seen in the damaged small bile ducts (SBDs) in PBC and the expression was significantly more frequent in PBC than in control livers (P < 0 |
23231002 | The accumulation of LC3-expressing punctae colocalized with PDC-E2 and CCO was significantly more increased in cultured BECs treated with various stresses |
23231002 | The cell-surface expression of PDC-E2 was induced by various stresses in BECs |
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