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WormBase Tree Display for Gene: WBGene00006942

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Name Class

WBGene00006942SMapS_parentSequenceF41D9
IdentityVersion1
NameCGC_namewrk-1Person_evidenceWBPerson260
Sequence_nameF41D9.3
Molecular_name (15)
Other_nameCELE_F41D9.3Accession_evidenceNDBBX284606
Public_namewrk-1
DB_infoDatabaseAceViewgeneXJ6
WormQTLgeneWBGene00006942
WormFluxgeneWBGene00006942
NDBlocus_tagCELE_F41D9.3
PanthergeneCAEEL|WormBase=WBGene00006942|UniProtKB=Q5WRR1
familyPTHR45080
NCBIgene181093
RefSeqproteinNM_001029478.5
NM_001029480.6
NM_001029477.6
NM_001373391.4
NM_001029476.4
TREEFAMTREEFAM_IDTF325699
TrEMBLUniProtAccH2KZN8
H2KZN9
A0A4V0ING2
Q8MPV0
Q5WRR1
UniProt_GCRPUniProtAccQ5WRR1
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:43WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classwrk
Allele (104)
Strain (20)
RNASeq_FPKM (74)
GO_annotation00003971
00003972
00003973
00003974
00003975
00003976
00003977
Ortholog (34)
ParalogWBGene00004372Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionwrk-1 encodes, by alternative splicing, at least three isoforms of aGPI-anchored immunoglobulin superfamily (IgSF) protein orthologous toDrosophila KLINGON, WRAPPER, CG7166, and CG13506; WRK-1 is expressed inthe pioneering embryonic motoneurons (eMNs) DA, DB, and DD; WRK-1expression in DA, DB, and DD is necessary and sufficient to preventfollower axons from inappropriately crossing the ventral midline; WRK-1also retards developmental changes in the outward current of maturingAIY interneurons; in addition to eMNs and AIY neurons, WRK-1 isexpressed in ASI and SMDV/D neurons, along with sheath and socket cells,intestine, the excretory gland cell, distal tip cells, and coelomocytes;wrk-1 transcription in AIY requires TTX-3, being greatly reduced in attx-3(ot22) mutant background; however, wrk-1 may not betranscriptionally activated by CEH-10/TTX-3 heterodimers, since wrk-1 lacks an AIY motif in its cis-regulatory sequences; WRK-1 binds VAB-1 orVAB-2 in vitro, and wrk-1(ok695) mutations fail to enhance vab-1 or atriple vab-2, efn-2, and efn-3 mutation, indicating that WRK-1 acts in concert with ephrins; wrk-1(ok695) null mutants exhibit midlinecrossover defects in the axons of HSN, PVQ, AV-type, and PVC neurons;wrk-1(ok695) and wrk-1(tm1099) mutant neurons have normal whole cellcapacitance but precociously altered their outward current from a slowlyactivating, sustained current to a rapidly-activating one; hypodermal misexpression of WRK-1 induces defects in PVQ axonal outgrowth, which are enhanced by a wrk-1(ok695) mutant background; wrk-1(ok695) mutationsenhance sax-3(ky123), indicating that WRK-1 and SAX-3 act in parallel.Paper_evidenceWBPaper00005064
WBPaper00024232
WBPaper00027182
WBPaper00028566
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated07 Jan 2008 00:00:00
Automated_descriptionPredicted to enable axon guidance receptor activity. Predicted to be involved in homophilic cell adhesion via plasma membrane adhesion molecules and synapse organization. Predicted to be located in axon; neuronal cell body; and plasma membrane. Expressed in several structures, including SMDVL; body ganglion; head neurons; hermaphrodite distal tip cell; and interfacial epithelial cell.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
Molecular_infoCorresponding_CDSF41D9.3a
F41D9.3b
F41D9.3c
F41D9.3e
F41D9.3f
Corresponding_CDS_historyF41D9.3d:wp271
Corresponding_transcriptF41D9.3a.1
F41D9.3b.1
F41D9.3c.1
F41D9.3e.1
F41D9.3f.1
Other_sequenceJI167162.1
CBC16075_1
Acan_isotig08406
Tcol_isotig17069
Associated_feature (22)
Experimental_infoRNAi_resultWBRNAi00046984Inferred_automaticallyRNAi_primary
WBRNAi00014740Inferred_automaticallyRNAi_primary
WBRNAi00090689Inferred_automaticallyRNAi_primary
Expr_patternExpr1761
Expr4281
Expr7829
Expr8842
Expr13214
Expr1012620
Expr1032956
Expr1150847
Expr2018072
Expr2036210
Drives_constructWBCnstr00001442
WBCnstr00001443
WBCnstr00001444
WBCnstr00001497
WBCnstr00001530
WBCnstr00013552
WBCnstr00034084
Construct_productWBCnstr00001497
WBCnstr00006614
WBCnstr00034084
Microarray_results (43)
Expression_cluster (185)
Interaction (21)
Map_infoMapXPosition-0.140944Error0.004413
PositivePositive_cloneF41D9Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4755
4975
5631
Pseudo_map_position
Reference (15)
RemarkSequence connection from [Hobert O]
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