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WormBase Tree Display for Gene: WBGene00009082

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Name Class

WBGene00009082SMapS_parentSequenceF23B12
IdentityVersion2
NameCGC_namedlat-1Person_evidenceWBPerson1983
WBPerson261
Sequence_nameF23B12.5
Molecular_nameF23B12.5
F23B12.5.1
CE09597
Other_nameCELE_F23B12.5Accession_evidenceNDBBX284605
Public_namedlat-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:49WBPerson1971EventImportedInitial conversion from CDS class of WS125
208 Dec 2011 12:14:43WBPerson2970Name_changeCGC_namedlat-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdlat
Allele (34)
StrainWBStrain00002401
WBStrain00001598
WBStrain00051672
WBStrain00051677
WBStrain00055610
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (40)
ParalogWBGene00007824Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00014054Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020950Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptiondlat-1 is orthologous to the human gene dihydrolipoyllysine acetyltransferase component of the pyruvate dehydrogenase complex, mitochondrial; dlat-1 is involved in embryo development and reproduction; dlat-1 is predicted to have dihydrolipoyllysine-residue acetyltransferase activity, based on protein domain information; dlat-1 is expressed in the pharynx, anal depressor muscle, nervous system, head, tail, reproductive system, intestine, and the body wall musculature.Paper_evidenceWBPaper00005654
WBPaper00006395
WBPaper00006525
WBPaper00025054
WBPaper00029359
WBPaper00045521
WBPaper00045688
WBPaper00045689
WBPaper00049100
Person_evidenceWBPerson151
Accession_evidenceEnsEMBLENSG00000150768
INTERPROIPR006257
IPR001078
IPR004167
Curator_confirmedWBPerson324
WBPerson1823
WBPerson567
Date_last_updated01 Jun 2017 00:00:00
Automated_descriptionPredicted to enable dihydrolipoyllysine-residue acetyltransferase activity. Predicted to be involved in acetyl-CoA biosynthetic process from pyruvate. Predicted to be located in mitochondrial matrix. Predicted to be part of mitochondrial pyruvate dehydrogenase complex. Expressed in several structures, including head and tail. Human ortholog(s) of this gene implicated in pyruvate decarboxylase deficiency. Is an ortholog of human DLAT (dihydrolipoamide S-acetyltransferase).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:3649Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2896)
Molecular_infoCorresponding_CDSF23B12.5
Corresponding_transcriptF23B12.5.1
Other_sequence (129)
Associated_featureWBsf653387
WBsf234949
WBsf234950
WBsf234951
Experimental_infoRNAi_resultWBRNAi00106959Inferred_automaticallyRNAi_primary
WBRNAi00071594Inferred_automaticallyRNAi_primary
WBRNAi00045381Inferred_automaticallyRNAi_primary
WBRNAi00033341Inferred_automaticallyRNAi_primary
WBRNAi00111113Inferred_automaticallyRNAi_primary
WBRNAi00096985Inferred_automaticallyRNAi_primary
WBRNAi00096925Inferred_automaticallyRNAi_primary
WBRNAi00025197Inferred_automaticallyRNAi_primary
WBRNAi00108040Inferred_automaticallyRNAi_primary
WBRNAi00008687Inferred_automaticallyRNAi_primary
Expr_patternChronogram184
Chronogram1100
Expr5834
Expr5835
Expr16128
Expr1023106
Expr1033956
Expr1149304
Expr2010939
Expr2029178
Drives_constructWBCnstr00002437
WBCnstr00004343
WBCnstr00032479
Construct_productWBCnstr00032479
Microarray_results (18)
Expression_cluster (132)
Interaction (247)
Map_infoMapVPosition6.3438
PositivePositive_cloneF23B12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027145
WBPaper00038491
WBPaper00049828
WBPaper00055090
WBPaper00057849
WBPaper00062388
RemarkMap position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene