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WormBase Tree Display for Gene: WBGene00009824

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Name Class

WBGene00009824SMapS_parentSequenceF47G4
IdentityVersion2
NameCGC_namegpdh-1Person_evidenceWBPerson1851
Sequence_nameF47G4.3
Molecular_nameF47G4.3
F47G4.3.1
CE18701
Other_nameCELE_F47G4.3Accession_evidenceNDBBX284601
Public_namegpdh-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
212 Sep 2006 10:48:07WBPerson2970Name_changeCGC_namegpdh-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgpdh
Allele (40)
StrainWBStrain00032072
WBStrain00048030
RNASeq_FPKM (74)
GO_annotation (19)
Ortholog (49)
ParalogWBGene00010778Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptiongpdh-1 encodes one of two C. elegans glycerol 3-phosphate dehydrogenases; gpdh-1 mRNA expression is upregulated in response to hypertonicity, suggesting that GPDH-1 does play a role in osmotic stress adaptation in C. elegans via glycerol biosynthesis; regulation of gpdh-1 expression is controlled, in part, by a pathway that includes the OSM-8 mucin and the PTR-23 Patched-like receptor.Paper_evidenceWBPaper00006432
WBPaper00038064
Curator_confirmedWBPerson1843
Date_last_updated20 Apr 2011 00:00:00
Automated_descriptionPredicted to enable glycerol-3-phosphate dehydrogenase (quinone) activity. Predicted to be involved in NADH oxidation and glycerol-3-phosphate metabolic process. Predicted to be located in cytosol. Predicted to be part of glycerol-3-phosphate dehydrogenase complex. Expressed in hypodermis and intestine. Human ortholog(s) of this gene implicated in Brugada syndrome 2. Is an ortholog of human GPD1 (glycerol-3-phosphate dehydrogenase 1) and GPD1L (glycerol-3-phosphate dehydrogenase 1 like).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:0110219Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:28956)
Molecular_infoCorresponding_CDSF47G4.3
Corresponding_transcriptF47G4.3.1
Other_sequenceGO238924.1
Associated_feature (14)
Experimental_infoRNAi_resultWBRNAi00032450Inferred_automaticallyRNAi_primary
WBRNAi00003699Inferred_automaticallyRNAi_primary
WBRNAi00113945Inferred_automaticallyRNAi_primary
WBRNAi00047681Inferred_automaticallyRNAi_primary
Expr_patternExpr3986
Expr1010915
Expr1034292
Expr1151522
Expr2012209
Expr2030445
Drives_constructWBCnstr00000751
WBCnstr00008693
WBCnstr00031890
WBCnstr00038242
Construct_productWBCnstr00031890
Microarray_results (19)
Expression_cluster (287)
Interaction (173)
Map_infoMapIPosition23.0163Error0.010903
PositivePositive_cloneF47G4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (32)
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