DLAT Gene
protein-coding GIFtS: 64
GCID: GC11P111895
|
|
dihydrolipoamide S-acetyltransferase (Previous symbol: DLTA)
| |
Aliases for DLAT gene
(According to
1HGNC,
2Entrez Gene,
3UniProtKB/Swiss-Prot,
4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc,
7Ensembl,
8DME,
9miRBase,
and/or 10fRNAdb) About This Section
|
| Aliases |
|---|
| Dihydrolipoamide S-Acetyltransferase1 2 | | PBC2 3 | | DLTA1 2 3 | | M2 Antigen Complex 70 KDa Subunit2 3 | | PDC-E21 2 3 | | EC 2.3.1.123 8 | | PDCE22 3 5 | | Dihydrolipoyllysine-Residue Acetyltransferase Component Of PyruvateDehydrogenase Complex Mitochondrial2 | | Dihydrolipoamide Acetyltransferase Component Of Pyruvate Dehydrogenase Complex2 3 | | Dihydrolipoyllysine-Residue Acetyltransferase Component Of PyruvateDehydrogenase Complex, Mitochondrial2 | | Pyruvate Dehydrogenase Complex Component E22 3 | | E2 Component Of Pyruvate Dehydrogenase Complex2 | | 70 KDa Mitochondrial Autoantigen Of Primary Biliary Cirrhosis2 3 | | EC 2.3.18 |
Export aliases for DLAT gene to outside databasesPrevious GC identifers: GC11P114248 GC11P113407 GC11P111929 GC11P111433 GC11P111401 GC11P107819 |
Summaries for DLAT gene(According to Entrez Gene,
Tocris Bioscience,
Wikipedia's
Gene Wiki,
PharmGKB,
UniProtKB/Swiss-Prot,
and/or
UniProtKB/TrEMBL)
About This Section
| Entrez Gene summary for DLAT: This gene encodes component E2 of the multi-enzyme pyruvate dehydrogenase complex (PDC). PDC resides in the innermitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A. The protein product of thisgene, dihydrolipoamide acetyltransferase, accepts acetyl groups formed by the oxidative decarboxylation of pyruvateand transfers them to coenzyme A. Dihydrolipoamide acetyltransferase is the antigen for antimitochondrial antibodies.These autoantibodies are present in nearly 95% of patients with the autoimmune liver disease primary biliary cirrhosis(PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein isabnormally distributed and overexpressed. PBC enventually leads to cirrhosis and liver failure. Mutations in this geneare also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lactic acidosis in infancy and earlychildhood.(provided by RefSeq, Oct 2009) UniProtKB/Swiss-Prot: ODP2_HUMAN, P10515Function: The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), andthereby links the glycolytic pathway to the tricarboxylic cycle Gene Wiki entry for DLAT (Dihydrolipoyl transacetylase)
|
Genomic Views for DLAT gene
(According to
GeneLoc and/or
HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to
UCSC (hg19) and
Ensembl (release 69),
Regulatory elements and Epigenetics data according to
QIAGEN,
SABiosciences, and/or
SwitchGear Genomics) About This Section
| RefSeq DNA sequence:- NC_000011.9 NC_018922.1 NT_033899.8
Regulatory elements: SABiosciences Regulatory transcription factor binding sites in the DLAT gene promoter: Max1 SREBP-1c MyoD CBF-C Evi-1 SREBP-1b SREBP-1a CBF-B CP1A CBF(2) Other transcription factors
Search SABiosciences Chromatin IP Primers for DLAT
Epigenetics:
|  | QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat DLAT |
Genomic Location: Genomic View: UCSC Golden Path with GeneCards custom track
Entrez Gene cytogenetic band: 11q23.1 Ensembl cytogenetic band: 11q23.1 HGNC cytogenetic band: 11q23.1DLAT Gene in genomic location: bands according to Ensembl, locations according to
(and/or Entrez Gene and/or Ensembl if different)

GeneLoc information about chromosome 11 GeneLoc Exon Structure GeneLoc location for GC11P111895: view genomic region
(about GC identifiers)
Start:
|
111,895,538 bp from pter |
End:
|
111,935,114 bp from pter |
Size:
|
39,577 bases |
Orientation:
|
plus strand |
|
Proteins for DLAT gene
(According to
1UniProtKB,
HORDE,
neXtProt,
Ensembl,
and/or Reactome,
Modification sites according to 2PhosphoSitePlus,
Specific Peptides from DME,
Protein expression images according to data from SPIRE MOPED and PaxDb,
RefSeq according to NCBI,
PDB rendering according to OCA and/or Proteopedia,
Recombinant Proteins
from
EMD Millipore,
R&D Systems,
GenScript,
Enzo Life Sciences,
OriGene,
Novus Biologicals,
Sino Biological,
ProSpec, and/or
Uscn,
Biochemical Assays by
EMD Millipore,
R&D Systems,
OriGene,
GenScript,
Cell Signaling Technology,
Enzo Life Sciences, and/or
Uscn,
Ontologies according to Gene
Ontology Consortium 01 Mar 2013 and
Entrez Gene,
Antibodies by
EMD Millipore,
R&D Systems,
GenScript,
Cell Signaling Technology,
OriGene,
Novus Biologicals,
Thermo Fisher Scientific,
Abcam, and/or
Uscn)
About This Section
| UniProtKB/Swiss-Prot: ODP2_HUMAN, P10515 (See
protein sequence)Recommended Name: Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex,mitochondrial precursor Size: 647 amino acids; 68997 Da
Cofactor: Binds 2 lipoyl cofactors covalently
Subunit: Part of the multimeric pyruvate dehydrogenase complex that contains multiple copies of pyruvate dehydrogenase(E1), dihydrolipoamide acetyltransferase (DLAT, E2) and lipoamide dehydrogenase (DLD, E3). These subunits are bound toan inner core composed of about 48 DLAT and 12 PDHX molecules. Interacts with PDK2 and PDK3
Subcellular location: Mitochondrion matrix
Sequence caution: Sequence=AAA62253.1; Type=Frameshift; Positions=449, 451, 455; Sequence=AAA62253.1;Type=Miscellaneous discrepancy; Note=Contaminating sequence. Sequence of unknown origin in the N-terminal part;
6/10 PDB 3D structures from and Proteopedia for DLAT (see all 10):1FYC (3D)
  1Y8N (3D)
  1Y8O (3D)
  1Y8P (3D)
  2DNE (3D)
  2PNR (3D)
 
Secondary accessions: Q16783 Q53EP3Explore the universe of human proteins at neXtProt for DLAT: NX_P10515
Post-translational modifications:
View modification sites using PhosphoSitePlus2View neXtProt modification sites for NX_P10515 4/10 DME Specific Peptides for DLAT (P10515) (see all 10)
DLAT Protein expression data from MOPED and PaxDb: About this image 
REFSEQ proteins: NP_001922.2 ENSEMBL proteins: ENSP00000280346 ENSP00000435374 ENSP00000376771 ENSP00000433432 ENSP00000442427 Reactome Protein details: P10515 Human Recombinant Protein Products:
Gene Ontology (GO): 4 cellular component terms (GO ID links to tree view): About this table
DLAT for ontologies About GeneDecksing
DLAT Antibody Products: Assay Products for DLAT: |
Protein
Domains / Families for DLAT gene(According to InterPro, ProtoNet,
UniProtKB, and/or BLOCKS,
Sets of similar genes according to GeneDecks)
About This Section
|
DLAT for domains About GeneDecksing
5/7 InterPro domains/families (see all 7):Graphical View of Domain Structure for InterPro Entry P10515ProtoNet protein and cluster: P10515 4 Blocks protein families: IPB000089 Biotin/lipoyl attachment IPB001078 Catalytic domain of components of various dehydrogenase complexes IPB003016 2-oxo acid dehydrogenase IPB004167 E3 binding domain
UniProtKB/Swiss-Prot: ODP2_HUMAN, P10515Similarity: Belongs to the 2-oxoacid dehydrogenase familySimilarity: Contains 2 lipoyl-binding domains |
Function for DLAT gene
(According to 1UniProtKB,
Genatlas,
LifeMap Discovery™,
IUBMB, and/or
2DME,
Human phenotypes from GenomeRNAi,
Animal models from MGI Mar 06 2013,
bound targets from SABiosciences,
miRNA Gene Targets from miRTarBase
shRNA from
OriGene,
RNAi from
EMD Millipore,
siRNAs from
OriGene,
QIAGEN,
microRNA from QIAGEN,
Gene Editing from DNA2.0,
Clones from EMD Millipore,
OriGene,
SwitchGear Genomics,
GenScript,
Sino Biological,
DNA2.0,
and Vector BioLabs,
Cell Lines from GenScript,
LifeMap BioReagents,
In Situ Hybridization Assays from Advanced Cell Diagnostics,
Ontologies according to Gene Ontology Consortium 01 Mar 2013 via
Entrez Gene.)
About This Section
| Function Summary: UniProtKB/Swiss-Prot: ODP2_HUMAN, P10515Function: The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), andthereby links the glycolytic pathway to the tricarboxylic cycleCatalytic activity: Acetyl-CoA + enzyme N(6)-(dihydrolipoyl)lysine = CoA + enzyme N(6)-(S-acetyldihydrolipoyl)lysineEnzyme Numbers (IUBMB): EC 2.3.1.121 2 EC 2.3.12
Clone Products: |  | Browse Clones for the Expression of Recombinant Proteins Available from EMD Millipore | |  | OriGene Myc/DDK tagged cDNA clones in CMV expression vector in human, mouse, rat for DLAT (see all 3) OriGene untagged cDNA clones in CMV expression vector in human, mouse, rat for DLAT OriGene custom cloning services – gene synthesis, subcloning, mutagenesis,
variant library, vector shuttling 
| |  | GenScript: all cDNA clones in your preferred vector: DLAT (NM_001931) | |  | Browse Sino Biological Human cDNA Clones | |  | DNA2.0 Custom Codon Optimized Gene
Synthesis Service for DLAT | |  | Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat DLAT  |
In Situ Assay Products: |
| Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for DLAT |
Gene Ontology (GO): 2 molecular function terms (GO ID links to tree view): About this table
DLAT for ontologies About GeneDecksing
2 GenomeRNAi human phenotypes for DLAT:
|
Pathways & Interactions for DLAT gene
(Pathways according to
EMD Millipore,
R&D Systems,
Cell Signaling Technology,
KEGG,
PharmGKB,
BioSystems,
Reactome,
Tocris Bioscience,
GeneGo (Thomson Reuters),
QIAGEN,
and/or UniProtKB,
Sets of similar genes according to GeneDecks,
Interaction Networks according to
SABiosciences,
and/or STRING,
Interactions according to 1UniProtKB,
2MINT,
3I2D, and/or
4STRING,
with links to IntAct and
Ensembl,
Ontologies according to Gene Ontology Consortium 01 Mar 2013 via
Entrez Gene).
About This Section
| Unified GeneCards pathways - 5/8 super-pathways (see all 8) About this table  See pathways by source
| Super-pathway | contained gene-specific pathways |
|---|
| 1 | TCA Cycle | | | 2 | Pyruvate metabolism | | | 3 | Metabolism | | | 4 | Glycolysis and gluconeogenesis (short map) | | | 5 | Glucose / Energy Metabolism | |
Pathway sources See GeneCards unified pathways Show all pathways
1
Cell Signaling Technology (CST) Pathway for DLAT 3 BioSystems Pathways for DLAT 
5
Reactome Pathways for DLAT
4
Kegg Pathways (Kegg details for DLAT):
DLAT for pathways About GeneDecksing
Interactions:
Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for DLAT
STRING Interaction
Network Preview (showing 5 interactants - click image to see 25)
 5/143 Interacting proteins for DLAT (P105152, 3 ENSP000002803464) via UniProtKB, MINT, STRING, and/or I2D (see all 143)About this table
Gene Ontology (GO): 5/9 biological process terms (GO ID links to tree view) (see all 9): About this table | GO ID | Qualified GO term | Evidence | PubMed IDs |
|---|
| GO:0006006 | glucose metabolic process |
IEA | -- | | GO:0006085 | acetyl-CoA biosynthetic process |
NAS | -- | | GO:0006086 | acetyl-CoA biosynthetic process from pyruvate |
-- | -- | | GO:0006090 | pyruvate metabolic process |
TAS | -- | | GO:0006096 | glycolysis |
-- | -- |
DLAT for ontologies About GeneDecksing
|
Drugs & Compounds for DLAT gene(Chemical Compounds according to UniProtKB, Enzo Life Sciences,
EMD Millipore, Tocris Bioscience
HMDB,
BitterDB, and/or
Novoseek, and Drugs according to
DrugBank,
Enzo Life Sciences, and/or
PharmGKB, with drugs/clinical trials/news
search links to CenterWatch)
About This Section
|
DLAT for compounds About GeneDecksing
Browse Tocris compounds for DLAT
10/11 HMDB Compounds for DLAT (see all 11) About this table
3 DrugBank Compounds for DLAT About this table
10/12 Novoseek chemical compound relationships for DLAT gene (see all 12) About this table
| Compound |
-log (P-Val) |
Hits |
PubMed IDs for Articles with Shared Sentences (# sentences) |
| 2-oxo acid |
95.1 |
37 |
9594621 (2), 9141421 (1), 10484012 (1), 10807519 (1) (see all 23) |
| dihydrolipoamide |
92.8 |
38 |
9620315 (3), 7890655 (2), 1370237 (2), 16049940 (2) (see all 24) |
| pyruvate |
91.8 |
200 |
7519986 (5), 14638692 (4), 7927255 (3), 7822313 (3) (see all 99) |
| alpha lipoic acid |
80.6 |
27 |
19003917 (5), 7519986 (2), 7821922 (1), 9089910 (1) (see all 15) |
| alpha-ketoglutarate |
75.6 |
20 |
9141421 (1), 10484012 (1), 12734383 (1), 2243228 (1) (see all 14) |
| acetyl-coa |
57.1 |
8 |
8557670 (3), 18184588 (1), 12411477 (1), 15491151 (1) (see all 5) |
| amino acid |
36.7 |
2 |
7521314 (1) |
| nadh |
21.6 |
5 |
8557670 (2), 15491151 (1), 18627174 (1) |
| adp |
19 |
2 |
10748134 (1), 12816949 (1) |
| lysine |
19 |
11 |
15558739 (3), 1701753 (2), 18563844 (1), 10209517 (1) (see all 5) |
Search CenterWatch for drugs/clinical trials and news about DLAT / ODP2 
|
Transcripts for DLAT gene(Secondary structures according to
fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene
(Build 235 Homo sapiens; Mar 10 2013) or GenBank, RefSeq according to Entrez Gene,
DOTS (version 10), and/or
AceView,
transcript ids from Ensembl
with links to UCSC,
exon structure from GeneLoc,
alternative splicing isoforms according to ASD and/or
ECgene,
RNAi Products from
EMD Millipore,
siRNAs from
OriGene,
QIAGEN,
shRNA from
OriGene,
microRNA from QIAGEN,
Tagged/untagged cDNA clones from
OriGene,
SwitchGear Genomics,
GenScript,
DNA2.0,
Vector BioLabs,
Primers from
OriGene,
SABiosciences, and/or
QIAGEN
) About This Section
| REFSEQ mRNAs for DLAT gene: NM_001931.4 Unigene Cluster for DLAT: Dihydrolipoamide S-acetyltransferase Hs.335551 [show with all ESTs]Unigene Representative Sequence: NM_0019316 Ensembl transcripts including schematic representations, and UCSC links where relevant: ENST00000280346(uc001pmo.3 uc010rwr.2 uc021qqn.1) ENST00000533297 ENST00000393051 ENST00000531306 ENST00000527231 ENST00000537636
Clone Products: |  | OriGene Myc/DDK tagged cDNA clones in CMV expression vector in human, mouse, rat for DLAT (see all 3) OriGene untagged cDNA clones in CMV expression vector in human, mouse, rat for DLAT OriGene custom cloning services – gene synthesis, subcloning, mutagenesis,
variant library, vector shuttling 
| |  | GenScript: all cDNA clones in your preferred vector: DLAT (NM_001931) | |  | DNA2.0 Custom Codon Optimized Gene
Synthesis Service for DLAT | |  | Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat DLAT  |
Additional cDNA sequence: AF317200.1 AK057299.1 AK223596.1 AK296274.1 AK297103.1 AK303930.1 AL832703.1 BC039084.1 X13822.1 Y00978.1 13 DOTS entries: DT.75168175 DT.95378651 DT.100721475 DT.95167732 DT.217357 DT.100793562 DT.120733901 DT.92438859 DT.453367 DT.100793560 DT.100793558 DT.100793563 DT.92058549 261 AceView cDNA sequences (see top 24): BQ184815 AK057299 AI570903 BF725774 CA313259 BU679072 CK823258 BM541380 AA457372 BE273936 BU159332 AW188637 BG261347 CR617020 CN482077 AA400968 CA844364 BX093967 AL559500 AI472203 BF939962 AI799356 CR613534 AI452538 BM966823 AA641655 CK823259 BM991840 AI969624 BQ024276 BU507759 AL559499 BQ929850 BU508456 BF971921 AI740632 CA844366 AA281656 CB135962 BQ187728 BM840376 BU568670 AA336525 AI824872 BU542326 AA315214 BG527498 AA639499 CF137346 BX452767 BQ220634 AL133725 X85590 AA631173 AW614019 BX426865 AL832703 X13822 AL565025 CD654287 AI291378 BF978872 BM840394 AI335753 BE889601 BP372989 BX433494 CB051515 AA830439 BE936075 BG390485 AA811344 AU127045 AA457421 AU126868 BP357743 BU166230 BU542604 AA281787 BI333861 CB957566 AI290401 AA854588 AA831974 CD644169 AA923665 BG528511 AU123632 AL079485 AI439819 AU143351 AA524468 AI492900 BU197312 AW237732 BM542685 BQ685429 BP872999 AA455346 BG288425 BM550587 AF317200 AA400884 BU608854 AW299740 CA450535 CK000770 BU543781 R02093 BQ425525 AL040276 BG503419 AA776989 CA849048 AW950165 N29901 N23208 BX491790 BG253201 BQ028213 BQ023230 T29022 AW440940 AA334879 BX500451 AI241790 BG778185 BM764235 W46504 BE875239 N55093 BU508163 AL559724 BU173809 BI092658 AI761322 AA551888 BM838027 AI912840 NM_001931 BX482468 BM454276 CK002752 BC039084 BM474719 BF692462 AA228079 BM760444 AI677952 AI376777 BX500304 AI343654 BM463514 BX280342 BX502880 AA227971 BP358023 BU935166 BG116733 BX498143 BG390907 AW236592 BF347317 BG385552 CB047251 AI700076 BG528072 BE542004 AW235135 BM048369 BG029748 BU429259 CF146214 R72354 W46396 AW136894 AA234145 BI260173 BE886058 BX502005 BF699210 BU597617 Y00978 AA082311 BI860937 BG385467 AW768966 BE902800 BG386765 CB128426 BX364130 BF038188 AL581280 AI478538 N99373 AI569123 N42953 R02205 BF698324 R44685 BE513176 BF240067 BM834206 AW498537 AL597426 BM455483 BI259164 C03439 BF103577 BI334849 AA176282 CA849046 CB047252 BI197293 BG257434 AA455345 AI627665 BE782268 CD613462 Z48500 AA234964 AA091346 BQ323257 AU160458 CD701599 AI419467 BF696111 BG719386 BI836946 H51225 J03866 AW023062 BE259547 BF528520 AI382333 BQ350219 N28789 BG258860 BU940361 BE784101 BF239804 AI933985 CB051514 H10160 BF696958 N77305 BU430824 AA176281 BQ229346 N58639 R19436 BQ323266 AL079484 AL533134 BE762989 M77924 BQ705982 BF796701 H10159 BG118604 BE304417 GeneLoc Exon Structure
4 Alternative Splicing Database (ASD) splice patterns (SP) for DLAT About this scheme
| ExUns: | 1 | ^ | 2a | · | 2b | ^ | 3 | ^ | 4a | · | 4b | ^ | 5 | ^ | 6 | ^ | 7 | ^ | 8 | ^ | 9 | ^ | 10 | ^ | 11 | ^ | 12 | ^ | 13 | ^ | 14a | · | 14b | |
| SP1: | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |
| SP2: | |   | |   | |   | |   | |   | |   | - |   | - |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |
| SP3: | |   | |   | |   | |   | |   | - |   | - |   | - |   | - |   | - |   | - |   | - |   | - |   | - |   | |   | |   | |   | |
| SP4: | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   | |   |
ECgene alternative splicing isoforms for DLAT
|
Expression for DLAT gene
(RNA expression data according to
H-InvDB,
NONCODE,
miRBase, and
RNAdb,
Expression images according to data from
BioGPS,
Illumina Human BodyMap, and
CGAP
SAGE,
Sets of similar genes according to GeneDecks,
in vivo and in vitro expression data from LifeMap Discovery™,
plus additional links to
Genevestigator, and/or
SOURCE, and/or
BioGPS, and/or
UniProtKB,
PCR Arrays from
SABiosciences,
Primers from
OriGene,
SABiosciences, and/or
QIAGEN,
In Situ Hybridization Assays from Advanced Cell Diagnostics)
About This Section
| DLAT expression in normal human tissues (normalized intensities) See probesets specificity/sensitivity at GeneAnnot About this imageBioGPS CGAP TAG: --
About this image See DLAT Protein Expression from SPIRE MOPED and PaxDB Genevestigator expression for DLAT
SOURCE GeneReport for Unigene cluster: Hs.335551 SABiosciences Expression via Pathway-Focused PCR Arrays including DLAT:
Primer Products: |  | OriGene genome-wide validated SYBR primer pairs in human, mouse, rat for DLAT Browse OriGene validated miRNA SYBR primer pairs
| |  | SABiosciences RT2 qPCR Primer Assay in human, mouse, rat DLAT | |  | QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat DLAT | |  | QIAGEN QuantiFast Probe-based Assays in human, mouse, rat DLAT | In Situ Assay Products: |
| Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for DLAT |
Orthologs for DLAT gene
(Orthologs according to
1,2HomoloGene (2older version, for species not in 1newer version),
3euGenes,
4SGD
,
5MGI Mar 06 2013,
with possible further links to
Flybase
and/or
WormBase,
and/or
6Ensembl pan taxonomic compara ,
Gene Trees according to Ensembl and
TreeFam)
About This Section
|
This gene was present in the common ancestor of eukaryotes.
Orthologs for DLAT gene from 9/37 species (see all 37) About this table
| Organism |
Taxonomic classification |
Gene |
Description |
Human Similarity |
Orthology Type |
Details |
chicken (Gallus gallus) |
Aves |
DLAT1 |
dihydrolipoamide S-acetyltransferase |
72.58(n) 78.12(a) |
  |
419796 XM_417933.3 XP_417933.2 |
lizard (Anolis carolinensis) |
Reptilia |
DLAT6 |
-- |
78(a) |
1 ↔ 1 |
GL343973.1(92243-106224) |
African clawed frog (Xenopus laevis) |
Amphibia |
LOC3983142 |
dihydrolipoamide acetyltransferase |
75.45(n) |
  |
AF430140.1 |
zebrafish (Danio rerio) |
Actinopterygii |
Dr.28102 |
Danio rerio dihydrolipoamide S-acetyltransferase (dlat) more |
77.53(n) |
  |
AY188775.1 |
fruit fly (Drosophila melanogaster) |
Insecta |
CG52611 , 3 |
dihydrolipoamide S-acetyltransferase3 CG52611 |
52(a)3 56.46(n)1 55.37(a)1 |
  |
27F63 340211 NM_135274.21 NP_609118.11 |
worm (Caenorhabditis elegans) |
Secernentea |
F23B12.53 dlat-11 |
dihyrolipoamide acetyltransferase component (pyruvate more3 Protein DLAT-11 |
53(a) (best of 2)3 55.83(n)1 55.9(a)1 |
  |
V(14448187-14449885)3 1799451 NM_074178.51 NP_506579.11 |
baker's yeast (Saccharomyces cerevisiae) |
Saccharomycetes |
LAT1(YNL071W)4 LAT11 |
Dihydrolipoamide acetyltransferase component (E2) of more4 Lat1p1 |
52.38(n)1 47(a)1 |
  |
14(491523-492971)4 8556531, 4 NP_014328.31 NP_014328.14 |
thale cress (Arabidopsis thaliana) |
eudicotyledons |
AT1G542201 |
dihydrolipoyllysine-residue acetyltransferase component more |
53.98(n) 49.65(a) |
  |
841863 NM_001036109.1 NP_001031186.1 |
rice (Oryza sativa) |
Liliopsida |
AK070846.12 |
-- |
71.7(n) |
  |
AK070846.1 |
ENSEMBL Gene Tree for DLAT (if available) TreeFam Gene Tree for DLAT (if available)  |
Paralogs for DLAT gene(Paralogs according to
1HomoloGene, 2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68) About This Section
| Paralogs for DLAT gene
- PDHX2 DBT2
1 SIMAP similar gene for DLAT using alignment to 6 protein entries: ODP2_HUMAN (see all proteins):PDHX
DLAT for paralogs About GeneDecksing
|
Genomic Variants for DLAT gene(SNPs/Variants according to the
1NCBI SNP Database,
2Ensembl,
3PupaSUITE,
UniProtKB, and
DNA2.0,
Linkage Disequilibrium by HapMap,
Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene
Mutation Database (HGMD) and the Locus Specific Mutation
Databases (LSDB), Blood group antigen gene mutations by BGMUT,
Resequencing Primers from QIAGEN,
Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
About This Section
|
| Genomic Data | Transcription Related Data | Allele Frequencies | | SNP ID | Valid | Clinical significance | Chr 11 pos | Sequence | # | AA Chg | Type | More | # | Allele freq | Pop | Total sample | More |
|---|
HapMap Linkage Disequilibrium report for DLAT (111895538 - 111935114 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions) Database of Genomic Variants (DGV) variations for DLAT: -- Human Gene Mutation Database (HGMD): DLAT
 | SABiosciences Cancer Mutation PCR Assays |
|  | QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing DLAT |
|
Disorders
/ Diseases for DLAT gene
(in which this Gene is Involved, According to MalaCards,
OMIM, UniProtKB,
the University of Copenhagen DISEASES
database, Novoseek,
Genatlas, GeneTests,
GAD,
HuGE Navigator,
and/or TGDB.)
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DLAT for disorders About GeneDecksing
OMIM gene information: 608770 OMIM disorders: 245348 UniProtKB/Swiss-Prot: ODP2_HUMAN, P10515
Note=Primary biliary cirrhosis is a chronic, progressive cholestatic liver disease characterized by thepresence of antimitochondrial autoantibodies in patients' serum. It manifests with inflammatory obliteration ofintra-hepatic bile duct, leading to liver cell damage and cirrhosis. Patients with primary biliary cirrhosis showautoantibodies against the E2 component of pyruvate dehydrogenase complex Defects in DLAT are the cause of pyruvate dehydrogenase E2 deficiency (PDHE2 deficiency) [MIM:245348]; alsoknown as lactic acidemia due to defect of E2 lipoyl transacetylase of the pyruvate dehydrogenase complex. Pyruvatedehydrogenase (PDH) deficiency is a major cause of primary lactic acidosis and neurological dysfunction in infancy andearly childhood. In this form of PDH deficiency episodic dystonia is the major neurological manifestation, with othermore common features of pyruvate dehydrogenase deficiency, such as hypotonia and ataxia, being less prominent 20/25 diseases for DLAT (see all 25): About MalaCardsprimary biliary cirrhosis lactic acidosis liver disease pyruvate decarboxylase deficiency lipoamide dehydrogenase deficiency mycobacterium gordonae ulnar neuropathy cholangitis sjogren's syndrome dilated cardiomyopathy hepatitis c hepatocellular carcinoma autoimmune hepatitis epididymitis hypotonia cardiomyopathy hepatitis vaginitis myopathy neuropathy
3 diseases from the University of Copenhagen DISEASES database for DLAT:Primary biliary cirrhosis Pyruvate decarboxylase deficiency Ulnar neuropathy 10/12 Novoseek disease relationships for DLAT gene (see all 12) About this table
Human Genome Epidemiology (HuGE) Navigator: DLAT (5 documents) Export disorders for DLAT gene to outside databases
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Publications for DLAT gene (in
PubMed.
Associations of this gene to articles via
1Entrez Gene,
2UniProtKB/Swiss-Prot,
3HGNC,
4GAD,
5PharmGKB,
6HMDB,
7DrugBank,
8UniProtKB/TrEMBL,
9 Novoseek, and/or
10fRNAdb)
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PubMed articles for DLAT gene, integrated from 9 sources (see all 188): (articles sorted by number of sources associating them with DLAT) | |  | Utopia: connect your pdf to the dynamic world of online information |
- Organization of the cores of the mammalian pyruvate dehydrogenase complex formed by E2 and E2 plus the E3-binding protein and their capacities to bind the E1 and E3 components. (PubMed id 14638692)1, 2, 9 Hiromasa Y....Roche T.E. (2004)
- Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency. (PubMed id 16049940)1, 2, 9 Head R.A.... Brown G.K. (2005)
- Crystal structure of pyruvate dehydrogenase kinase 3 bound to lipoyl domain 2 of human pyruvate dehydrogenase complex. (PubMed id 15861126)1, 2 Kato M.... Chuang D.T. (2005)
- Three-dimensional structure of the major autoantigen in primary biliary cirrhosis. (PubMed id 9649469)1, 2 Howard M.J.... Yeaman S.J. (1998)
- Chromosome localization and RFLP analysis of PDC-E2: the major autoantigen of primary biliary cirrhosis. (PubMed id 8102256)1, 3 Leung P.S....Gershwin M.E. (1993)
- Primary structure of the human M2 mitochondrial autoantigen of primary biliary cirrhosis: dihydrolipoamide acetyltransferase. (PubMed id 3174635)1, 2 Coppel R.L.... Gershwin M.E. (1988)
- Nucleotide sequence of a cDNA for the dihydrolipoamide acetyltransferase component of human pyruvate dehydrogenase complex. (PubMed id 3191998)1, 2 Thekkumkara T.J.... Patel M.S. (1988)
- Catalytic domain of PDC-E2 contains epitopes recogniz ed by antimitochondrial antibodies in primary biliary cirrhosis. (PubMed id 20180236)1, 9 Braun S....Klein R. (2010)
- Apotopes and the biliary specificity of primary biliary cirrhosis. (PubMed id 19185000)1, 9 Lleo A....Gershwin M.E. (2009)
- Comprehensive mapping of HLA-A0201-restricted CD8 T-cell epitopes on PDC-E2 in primary biliary cirrhosis. (PubMed id 12395322)1, 9 Matsumura S....Gershwin M.E. (2002)
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External Searches for DLAT gene
(in PubMed,
OMIM, and NCBI Bookshelf) About This Section
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Genome Databases showing DLAT gene
(According to
Entrez Gene,
HGNC,
AceView,
euGenes,
Ensembl,
miRBase,
ECgene,
Kegg,
and/or
H-InvDB)
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Other Databases showing DLAT gene
(According to HUGE)
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Specialized Databases showing DLAT gene(According to PharmGKB,
ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL, Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot) About This Section
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| Name | Description |
| PharmGKB entry for DLAT | Pharmacogenomics, SNPs, Pathways |
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| Patent Information for DLAT gene: Search GeneIP for patents involving DLAT
GeneCards and IP: Japan Patent Office Licenses GeneCards European Patent Office Licenses GeneCards Improving the IP Search
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Products for DLAT gene(Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or
Enzo Life Sciences), In Situ Hybridization Assays from Advanced Cell Diagnostics About This Section
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