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WormBase Tree Display for Gene: WBGene00004258

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Name Class

WBGene00004258SMapS_parentSequenceD2023
IdentityVersion1
NameCGC_namepyc-1Person_evidenceWBPerson184
Sequence_nameD2023.2
Molecular_nameD2023.2a
D2023.2a.1
CE09072
D2023.2b
CE46773
D2023.2a.2
D2023.2b.1
Other_nameCELE_D2023.2Accession_evidenceNDBBX284605
Public_namepyc-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpyc
Allele (66)
StrainWBStrain00054654
RNASeq_FPKM (74)
GO_annotation (22)
Ortholog (39)
ParalogWBGene00050970Caenorhabditis elegansFrom_analysismodENCODE_Pseudogenes
WBGene00004076Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00009319Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00012131Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00017864Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionpyc-1 encodes the C. elegans pyruvate carboxylase ortholog; by homology, PYC-1 is predicted to function as a key regulatory enzyme of gluconeogenesis, lipogenesis, and anaplerosis, localizing to the mitochondrial matrix and catalyzing the formation of oxaloacetate from pyruvate and carbonate; pyc-1 expression is induced upon exposure of C. elegans to cadmium.Paper_evidenceWBPaper00004992
WBPaper00005654
Curator_confirmedWBPerson1843
Date_last_updated16 Oct 2011 00:00:00
Automated_descriptionPredicted to enable pyruvate carboxylase activity. Predicted to be involved in gluconeogenesis and pyruvate metabolic process. Located in mitochondrion. Human ortholog(s) of this gene implicated in pyruvate carboxylase deficiency disease. Is an ortholog of human PC (pyruvate carboxylase).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:3651Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8636)
Disease_relevanceMutations in human pyruvate carboxylase (PC) lead to pyruvate carboxylase deficiency, and are also associated with lactic acidemia, neurological abnormalities, and early death; in elegans, pyc-1, orthologous to PC, is a cadmium-responsive gene.Homo sapiensPaper_evidenceWBPaper00004992
Accession_evidenceOMIM266150
608786
Curator_confirmedWBPerson324
Date_last_updated03 Aug 2013 00:00:00
Molecular_infoCorresponding_CDSD2023.2a
D2023.2b
Corresponding_transcriptD2023.2a.1
D2023.2a.2
D2023.2b.1
Other_sequence (114)
Associated_feature (19)
Experimental_infoRNAi_resultWBRNAi00043452Inferred_automaticallyRNAi_primary
WBRNAi00092274Inferred_automaticallyRNAi_primary
WBRNAi00111119Inferred_automaticallyRNAi_primary
WBRNAi00092273Inferred_automaticallyRNAi_primary
WBRNAi00012571Inferred_automaticallyRNAi_primary
WBRNAi00030388Inferred_automaticallyRNAi_primary
Expr_patternExpr1017480
Expr1032101
Expr1147446
Expr2015202
Expr2033436
Drives_constructWBCnstr00035605
Construct_productWBCnstr00035605
Microarray_results (18)
Expression_cluster (149)
Interaction (66)
Map_infoMapVPosition3.38497Error0.002077
PositivePositive_cloneD2023Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (13)
Remarksequence connection from [Freedman JH]
Map 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