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WormBase Tree Display for Gene: WBGene00006746

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Name Class

WBGene00006746SMapS_parentSequenceF41C6
IdentityVersion1
NameCGC_nameunc-6Person_evidenceWBPerson261
Sequence_nameF41C6.1
Molecular_nameF41C6.1
F41C6.1.1
CE04538
F41C6.1.2
Other_nameunc-106
CELE_F41C6.1Accession_evidenceNDBBX284606
Public_nameunc-6
DB_infoDatabaseAceViewgeneXH515
WormQTLgeneWBGene00006746
WormFluxgeneWBGene00006746
NDBlocus_tagCELE_F41C6.1
PanthergeneCAEEL|WormBase=WBGene00006746|UniProtKB=P34710
familyPTHR10574
NCBIgene180961
RefSeqproteinNM_076764.5
SwissProtUniProtAccP34710
UniProt_GCRPUniProtAccP34710
OMIMgene601614
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:41WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00142950
Allele (130)
Legacy_informatione78 : slight kinker poor backing large healthy slightly fat; dorsal extensions of DD and VD neurons grow in aberrant directions fail to reach dorsal cord; ventral cord disorganized etc. ES3 ME1. NA4 (e7 e181 ev400 (pka unc-106 : uncoordinated high frequency of phasmid axon displacement)).
See unc-6.
See also ev400, n102, n165, n593, n594
[C.elegansII] e78 : slight kinker, poor backing; large, healthy, slightly fat; dorsal extensions of DD and VD neurons grow in aberrant directions fail to reach dorsal cord; ventral cord disorganized; abnormal gonad arms, etc. ES3 ME1. OA>20: e7, e181, ev400 (pka unc-106,uncoordinated, high frequency of phasmid axon displacement), n593, n594 etc. Some alleles (rh202, rh204, rh402 etc.) defective only in dorsalward migrations. Null alleles defective in both dorsalward and ventralward migrations. See also unc-5, unc-40. Cloned: encodes extracellular matrix component, laminin-related at N-term, homologous to vertebrate netrins. [Ishii et al. 1992; NW]
Strain (70)
RNASeq_FPKM (74)
GO_annotation (60)
Ortholog (43)
ParalogWBGene00001328Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00002247Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00002248Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006432Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006787Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00018304Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00016913Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020581Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionunc-6 encodes a netrin orthologous to the human and mouse netrin-1 precursor proteins; UNC-6 functions as a guidance molecule that regulates circumferential axon migrations as well as migration of mesodermal cells, such as the gonadal distal tip cell, along the dorsoventral axis; in addition, UNC-6 mediates anchor cell (AC) invasion by regulating localization of the UNC-40 netrin receptor to the invasive plasma membrane of the AC, allowing for subsequent formation of an invasive membrane domain; a secreted molecule, UNC-6 is first expressed during embryogenesis in ventral epidermoblasts; additional expression is seen in neurons and sheath cells; UNC-6 is involved in both attractive and repulsive interactions mediated by the UNC-40 and UNC-5 netrin receptors, respectively.Paper_evidenceWBPaper00002378
WBPaper00003642
WBPaper00004938
WBPaper00005417
WBPaper00005809
WBPaper00027335
WBPaper00032446
Curator_confirmedWBPerson1843
Date_last_updated25 Aug 2009 00:00:00
Automated_descriptionPredicted to enable signaling receptor binding activity. Involved in several processes, including axon guidance; regulation of locomotion; and sex differentiation. Acts upstream of or within dendrite morphogenesis. Located in axon; basement membrane; and cytoplasm. Expressed in several structures, including P1; VA12; accessory cell; interneuron; and somatic neurons. Human ortholog(s) of this gene implicated in congenital mirror movement disorder. Is an ortholog of human NTN1 (netrin 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_modelDOID:0111153Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8029)
Molecular_infoCorresponding_CDSF41C6.1
Corresponding_transcriptF41C6.1.1
F41C6.1.2
Other_sequence (22)
Associated_feature (17)
Experimental_infoRNAi_result (13)
Expr_patternChronogram678
Expr1590
Expr6024
Expr8561
Expr9253
Expr13722
Expr13723
Expr13724
Expr14553
Expr1010621
Expr1032820
Expr1150827
Expr2017900
Expr2036036
Drives_construct (24)
Construct_product (30)
Microarray_results (22)
Expression_cluster (182)
Interaction (245)
Anatomy_functionWBbtf0504
WBbtf0505
WBProcessWBbiopr:00000025
Map_infoMapXPosition-2.07556Error0.040208
Well_ordered
PositiveInside_rearrstDp2
mnDp30
Positive_cloneF41C6Inferred_automaticallyFrom sequence, transcript, pseudogene data
NJ#14
NegativeOutside_rearrmcDf2
Mapping_data2_point150
165
177
178
185
188
236
237
3385
7093
Multi_point (67)
Pos_neg_data (20)
Landmark_gene
Reference (412)
MethodGene