Gene Gene information from NCBI Gene database.
Entrez ID 1737
Gene name Dihydrolipoamide S-acetyltransferase
Gene symbol DLAT
Synonyms (NCBI Gene)
DLTAE2PBCPDC-E2PDCE2
Chromosome 11
Chromosome location 11q23.1
Summary This gene encodes component E2 of the multi-enzyme pyruvate dehydrogenase complex (PDC). PDC resides in the inner mitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A. The protein product of this gene, dihydrolipoamide acet
SNPs SNP information provided by dbSNP.
7
SNP ID Visualize variation Clinical significance Consequence
rs138505899 T>G Likely-pathogenic Coding sequence variant, intron variant, 5 prime UTR variant, missense variant, non coding transcript variant
rs140678772 G>A Conflicting-interpretations-of-pathogenicity Coding sequence variant, non coding transcript variant, intron variant, missense variant
rs367875541 G>A Likely-pathogenic Splice acceptor variant
rs781936816 G>A Conflicting-interpretations-of-pathogenicity Synonymous variant, intron variant, non coding transcript variant, coding sequence variant, 5 prime UTR variant
rs782070173 T>C Likely-pathogenic Splice donor variant
miRNA miRNA information provided by mirtarbase database.
184
miRTarBase ID miRNA Experiments Reference
MIRT032242 hsa-let-7b-5p Proteomics 18668040
MIRT047485 hsa-miR-10b-5p CLASH 23622248
MIRT040451 hsa-miR-615-3p CLASH 23622248
MIRT447438 hsa-miR-5192 PAR-CLIP 22100165
MIRT447439 hsa-miR-6731-5p PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
35
GO ID Ontology Definition Evidence Reference
GO:0004742 Function Dihydrolipoyllysine-residue acetyltransferase activity IBA
GO:0004742 Function Dihydrolipoyllysine-residue acetyltransferase activity IDA 9045657, 9242632, 20160912
GO:0004742 Function Dihydrolipoyllysine-residue acetyltransferase activity IEA
GO:0004742 Function Dihydrolipoyllysine-residue acetyltransferase activity NAS 3191998
GO:0004742 Function Dihydrolipoyllysine-residue acetyltransferase activity TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608770 2896 ENSG00000150768
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P10515
Protein name Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial (EC 2.3.1.12) (70 kDa mitochondrial autoantigen of primary biliary cirrhosis) (PBC) (Dihydrolipoamide acetyltransferase component of pyruvate dehydrog
Protein function As part of the pyruvate dehydrogenase complex, catalyzes the transfers of an acetyl group to a lipoic acid moiety (Probable). The pyruvate dehydrogenase complex, catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and thereby l
PDB 1FYC , 1Y8N , 1Y8O , 1Y8P , 2DNE , 2PNR , 2Q8I , 3B8K , 3CRK , 3CRL , 6CT0 , 6H55 , 8PIU
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00364 Biotin_lipoyl 92 165 Biotin-requiring enzyme Domain
PF00364 Biotin_lipoyl 219 293 Biotin-requiring enzyme Domain
PF02817 E3_binding 355 390 e3 binding domain Family
PF00198 2-oxoacid_dh 417 647 2-oxoacid dehydrogenases acyltransferase (catalytic domain) Domain
Sequence
Sequence length 647
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
239
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Pancreatic adenocarcinoma Pathogenic rs782185799 RCV005931608
Pyruvate dehydrogenase E2 deficiency Likely pathogenic; Pathogenic rs1432866316, rs2137679109, rs1862823765, rs1862000857, rs782029228, rs782185799, rs782225633, rs2498425963, rs367875541, rs782704553, rs781991355 RCV001844333
RCV000002190
RCV003498718
RCV003603261
RCV003603203
RCV003603410
RCV003603997
RCV004547317
RCV001196727
RCV000500244
RCV002633576
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Likely benign rs144235197 RCV005892932
Cholangiocarcinoma Benign; Likely benign rs143107853 RCV005890734
DLAT-related disorder Benign; Likely benign rs61757217, rs782078082, rs781917992, rs781840468, rs144235197, rs368477013, rs199835215, rs782157762 RCV003975102
RCV003926290
RCV003903450
RCV003961330
RCV003977872
RCV003911455
RCV003930279
RCV003928001
Familial cancer of breast Likely benign rs144235197 RCV005891941
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Stimulate 36949759
Alcohol Related Disorders Associate 36611155, 37505170
Arthritis Psoriatic Associate 16622521
Arthritis Rheumatoid Associate 37547319
Breast Neoplasms Associate 35996075, 36949759, 37180167
Breast Neoplasms Inhibit 36312586
Carcinogenesis Associate 36949759, 37199628, 37949877
Carcinoma Hepatocellular Associate 36611155, 37124062, 37885090, 37949877, 38025761, 38078880, 39528670, 40141422
Carcinoma Hepatocellular Stimulate 36949759, 37828099, 39710381
Carcinoma Non Small Cell Lung Associate 35869499