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WormBase Tree Display for Gene: WBGene00010362

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Name Class

WBGene00010362SMapS_parentSequenceH04D03
IdentityVersion3
NameCGC_nameenu-3.1Person_evidenceWBPerson3027
Sequence_nameH04D03.1
Molecular_nameH04D03.1
H04D03.1.1
CE16165
Other_nameenu-3Person_evidenceWBPerson3027
CELE_H04D03.1Accession_evidenceNDBBX284603
Public_nameenu-3.1
DB_infoDatabaseAceViewgene3L527
WormQTLgeneWBGene00010362
WormFluxgeneWBGene00010362
NDBlocus_tagCELE_H04D03.1
PanthergeneCAEEL|WormBase=WBGene00010362|UniProtKB=O45607
familyPTHR31026
NCBIgene176463
RefSeqproteinNM_066901.6
TREEFAMTREEFAM_IDTF316689
TrEMBLUniProtAccO45607
UniProt_GCRPUniProtAccO45607
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
208 Feb 2011 16:27:44WBPerson2970Name_changeCGC_nameenu-3
328 Apr 2014 11:13:08WBPerson2970Name_changeCGC_nameenu-3.1
Other_nameenu-3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classenu
AlleleWBVar00531929
WBVar01500260
WBVar02034241
WBVar00407328
WBVar00407329
WBVar00407330
WBVar00407331
WBVar00407332
WBVar01918770
WBVar01499194
WBVar01645959
WBVar01499774
WBVar01499594
WBVar01499595
WBVar00269978
WBVar00856465
WBVar00856466
WBVar00856467
WBVar00856468
WBVar00856469
WBVar00856470
WBVar00856471
WBVar00856472
WBVar00856473
WBVar00856474
WBVar00252950
WBVar01332798
WBVar01332799
WBVar01952613
WBVar02036297
WBVar01802382
RNASeq_FPKM (74)
GO_annotation00034852
00034853
00034854
00034855
00034856
00034857
00034858
Ortholog (21)
ParalogWBGene00008003Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00012552Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00021015Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00021034Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WBGene00010477Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionenu-3 encodes a novel protein containing a single transmembrane domain and, at 144-165 amino acids, a coiled-coil region; enu-3 mutations enhance the axonal outgrowth defects of unc-5, although enu-3 mutations alone cause no motor axon outgrowth defects; ENU-3 functions in the same pathway as UNC-5 and UNC-6 for motor axon guidance to the dorsal cord but in a pathway parallel to UNC-5 and UNC-6 for axon outgrowth; enu-3 mutants are mildly uncoordinated and have a slight egg-laying defective phenotype; the rescue of axon outgrowth defects of a strain lacking both ENU-3 and UNC-5 depended on the presence of functional ENU-3 protein; ENU-3 is expressed in the PVT interneuron and is weakly expressed in many cell bodies along the ventral cord, including those of the DA and DB motor neurons.Paper_evidenceWBPaper00038105
Curator_confirmedWBPerson12884
Date_last_updated02 Jun 2011 00:00:00
Automated_descriptionInvolved in axon extension involved in axon guidance. Located in neuronal cell body. Expressed in head; nervous system; and seam 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_CDSH04D03.1
Corresponding_transcriptH04D03.1.1
Associated_featureWBsf994020
WBsf1015786
WBsf225719
WBsf225720
Experimental_infoRNAi_result (27)
Expr_patternExpr9239
Expr14491
Expr1024584
Expr1034524
Expr1153023
Expr2011330
Expr2029566
Drives_constructWBCnstr00008437
WBCnstr00008438
WBCnstr00008440
WBCnstr00013845
WBCnstr00019907
WBCnstr00031469
Construct_productWBCnstr00008437
WBCnstr00008439
WBCnstr00008440
WBCnstr00013845
WBCnstr00031469
WBCnstr00040912
Microarray_results (18)
Expression_cluster (142)
Interaction (20)
Map_infoMapIIIPosition2.50169Error0.003023
PositivePositive_cloneH04D03Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038105
WBPaper00044299
WBPaper00047925
WBPaper00051476
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