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WormBase Tree Display for Gene: WBGene00011510

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Name Class

WBGene00011510SMapS_parentSequenceT05H10
IdentityVersion2
NameCGC_namepdha-1Person_evidenceWBPerson1983
WBPerson261
Sequence_nameT05H10.6
Molecular_nameT05H10.6a
T05H10.6a.1
CE01643
T05H10.6b
CE32929
T05H10.6a.2
T05H10.6a.3
T05H10.6b.1
Other_nameCELE_T05H10.6Accession_evidenceNDBBX284602
Public_namepdha-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:52WBPerson1971EventImportedInitial conversion from CDS class of WS125
208 Dec 2011 12:14:43WBPerson2970Name_changeCGC_namepdha-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpdha
Allele (19)
StrainWBStrain00051190
WBStrain00051904
RNASeq_FPKM (74)
GO_annotation (16)
Contained_in_operonCEOP2336
Ortholog (51)
ParalogWBGene00012713Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionT05H10.6 encodes an ortholog of the human gene PYRUVATE DEHYDROGENASE (LIPOAMIDE) ALPHA 1 (PDHA1; OMIM:312170), which when mutated leads to Leigh syndrome (OMIM:256000).Paper_evidenceWBPaper00004424
WBPaper00004637
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable pyruvate dehydrogenase (acetyl-transferring) activity. Predicted to be involved in acetyl-CoA biosynthetic process from pyruvate. Located in mitochondrion. Human ortholog(s) of this gene implicated in pyruvate decarboxylase deficiency and spermatogenic failure. Is an ortholog of human PDHA1 (pyruvate dehydrogenase E1 subunit alpha 1) and PDHA2 (pyruvate dehydrogenase E1 subunit alpha 2).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:0111910Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8807)
DOID:3649Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8806)
Molecular_infoCorresponding_CDST05H10.6a
T05H10.6b
Corresponding_transcriptT05H10.6a.1
T05H10.6a.2
T05H10.6a.3
T05H10.6b.1
Other_sequence (156)
Associated_featureWBsf657930
WBsf221680
WBsf221681
WBsf221682
Experimental_infoRNAi_result (24)
Expr_patternExpr1025242
Expr1035071
Expr1156193
Expr2014802
Expr2033036
Drives_constructWBCnstr00030600
Construct_productWBCnstr00030600
Microarray_results (30)
Expression_cluster (108)
Interaction (78)
Map_infoMapIIPosition0.661005
PositivePositive_cloneT05H10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027145
WBPaper00031648
WBPaper00038491
WBPaper00044730
WBPaper00049828
WBPaper00055090
WBPaper00056909
WBPaper00059520
WBPaper00060084
WBPaper00065824
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