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WormBase Tree Display for Gene: WBGene00017089

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Name Class

WBGene00017089SMapS_parentSequenceE01A2
IdentityVersion2
NameCGC_namepoml-2Person_evidenceWBPerson10017
WBPerson95
Sequence_nameE01A2.7
Molecular_nameE01A2.7
E01A2.7.1
CE24874
Other_nameCELE_E01A2.7Accession_evidenceNDBBX284601
Public_namepoml-2
DB_infoDatabaseAceViewgene1E712
WormQTLgeneWBGene00017089
WormFluxgeneWBGene00017089
NDBlocus_tagCELE_E01A2.7
PanthergeneCAEEL|WormBase=WBGene00017089|UniProtKB=Q966L1
familyPTHR11799
NCBIgene171999
RefSeqproteinNM_058905.5
TREEFAMTREEFAM_IDTF322436
TrEMBLUniProtAccQ966L1
UniProt_GCRPUniProtAccQ966L1
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
213 Apr 2012 16:55:20WBPerson2970Name_changeCGC_namepoml-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpoml
Allele (30)
StrainWBStrain00032254
RNASeq_FPKM (74)
GO_annotation00091003
00091004
00122569
Ortholog (57)
ParalogWBGene00003170Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00010775Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00077701Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00044697Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionThe E01A2.7 gene encodes one of five paraoxonase-like proteins; it is homologous to the human genes PARAOXONASE 1 gene (PON1, OMIM:168820) and PARAOXONASE 2 (OMIM:602447), which in some allelic forms are associated with susceptibility to coronary artery disease or to variations in fasting plasma glucose.Paper_evidenceWBPaper00005591
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable arylesterase activity and metal ion binding activity. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; autoimmune disease (multiple); eye disease (multiple); and hematologic cancer (multiple). Is an ortholog of human PON1 (paraoxonase 1).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_model (48)
Molecular_infoCorresponding_CDSE01A2.7
Corresponding_transcriptE01A2.7.1
Other_sequenceOden_isotig15033
CJC01469_1
Tcir_isotig22284
Oden_isotig15034
FK802982.1
ES413786.1
Associated_featureWBsf664125
WBsf219243
Experimental_infoRNAi_resultWBRNAi00043561Inferred_automaticallyRNAi_primary
WBRNAi00033607Inferred_automaticallyRNAi_primary
WBRNAi00023692Inferred_automaticallyRNAi_primary
WBRNAi00023396Inferred_automaticallyRNAi_primary
WBRNAi00023980Inferred_automaticallyRNAi_primary
WBRNAi00023180Inferred_automaticallyRNAi_primary
WBRNAi00003308Inferred_automaticallyRNAi_primary
Expr_patternExpr1013081
Expr1037347
Expr1147555
Expr2014997
Expr2033232
Drives_constructWBCnstr00027577
Construct_productWBCnstr00027577
Microarray_results (19)
Expression_cluster (155)
InteractionWBInteraction000123689
WBInteraction000123690
Map_infoMapIPosition-1.69879
PositivePositive_cloneE01A2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00065080
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