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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_sequenceAF237467
SS00884
CRC04580_1
CR01133
MI03719
EX558642.1
Acan_isotig12228
BUC00504_1
Dviv_isotig16068
Name_isotig02236
HG04348
Oden_isotig01452
FK802249.1
CRC02654_1
RSC03785_1
EX913332.1
SSC01413_1
HBC20509_1
CJC07645_1
CBC02533_1
GO252677.1
BXC06431_1
RS11398
XI02489
EY471178.1
Dviv_isotig16069
EX535995.1
ES414162.1
EX547805.1
FK803677.1
CR03668
CR11709
HG00905
HG11248
EX909986.1
EX537016.1
HBC02157_1
Acan_isotig17566
EX537743.1
Tcir_isotig08167
RS07931
CR10941
FG589607.1
EY464715.1
HG07816
Oden_isotig01453
HGC11182_1
ACC12444_1
CJC15330_1
CJC01808_1
FC817755.1
TS03467
MI00443
TS01403
TDC00869_1
BUC01486_1
RSC01677_1
MIC00991_1
MI01291
ES409444.1
GO250503.1
HGC03069_1
EX566395.1
TSC00106_1
EX548198.1
Name_isotig03108
HGC09507_1
CGC01339_1
AYC00126_1
EX552992.1
CRC04768_1
HBC16975_1
SRC02883_1
GO251748.1
CBC07604_1
HGC03271_1
HBC24245_1
SS00117
JI164848.1
PPC01550_1
BXC03476_1
ES413364.1
EX538146.1
Acan_isotig07671
Hbac_isotig01127
EX555821.1
EX543309.1
SSC03570_1
FK805413.1
BUC01051_1
Name_isotig07827
PP02403
Hbac_isotig05407
EX557958.1
Tcol_contig04497
HS01168
EY465255.1
EX566028.1
EX564173.1
SSC06514_1
SR02981
EX566790.1
HSC01524_1
MIC00390_1
PPC00056_1
SS00154
AE01686
ACC09725_1
CB038490.1
Oden_isotig01454
ES409641.1
PPC18260_1
Tcol_isotig00759
XIC03081_1
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