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WormBase Tree Display for Gene: WBGene00004854

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Name Class

WBGene00004854SMapS_parentSequenceCHROMOSOME_X
IdentityVersion1
NameCGC_nameslt-1Person_evidenceWBPerson42
Sequence_nameF40E10.4
Molecular_nameF40E10.4
F40E10.4.1
CE32412
Other_nameCELE_F40E10.4Accession_evidenceNDBBX284606
Public_nameslt-1
DB_infoDatabaseAceViewgeneXP301
WormQTLgeneWBGene00004854
WormFluxgeneWBGene00004854
NDBlocus_tagCELE_F40E10.4
PanthergeneCAEEL|WormBase=WBGene00004854|UniProtKB=G5EFX6
familyPTHR45836
NCBIgene181562
RefSeqproteinNM_078036.8
SwissProtUniProtAccG5EFX6
TREEFAMTREEFAM_IDTF332887
UniProt_GCRPUniProtAccG5EFX6
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classslt
AlleleWBVar00145282Inferred_automaticallyFrom strain object: CX5347
WBVar01499887
WBVar01499519
WBVar01499888
WBVar01209823
WBVar02151799
WBVar01209824
WBVar01693724
WBVar01209825
WBVar01499710
WBVar01209826
WBVar01209827
WBVar01527977
WBVar01788180
WBVar01209828
WBVar01788181
WBVar01527978
WBVar01209829
WBVar01209830
WBVar01527979
WBVar01527980
WBVar01209831
WBVar01527981
WBVar01209832
WBVar01209833
WBVar01527982
WBVar01209834
WBVar01527983
WBVar01527984
WBVar01209835
WBVar01209836
WBVar01527985
WBVar01209837
WBVar01488128
WBVar01527986
WBVar01527987
WBVar01209838
WBVar01209839
WBVar01209840
WBVar01209841
WBVar01545011
WBVar01545012
WBVar01209842
WBVar01209843
WBVar01209844
WBVar00249355
WBVar01494944
WBVar01209845
WBVar01209846
WBVar01209847
WBVar01209848
WBVar01209849
WBVar01209850
WBVar01209851
WBVar01209852
WBVar01209853
WBVar01209854
WBVar01209855
WBVar00218639
WBVar01209856
WBVar00218640
WBVar00145128
WBVar00218641
WBVar01209857
WBVar00218643
WBVar01209858
WBVar01209859
WBVar00218644
WBVar01209860
WBVar00218645
WBVar01209861
WBVar00218646
WBVar01209862
WBVar00218647
WBVar01209863
WBVar01209864
WBVar01209865
WBVar01704291
WBVar01209866
WBVar01573118
WBVar01704292
WBVar01209867
WBVar01573119
WBVar01209868
WBVar01573120
WBVar01209869
WBVar01209870
WBVar01209871
WBVar01209872
WBVar01209873
WBVar01209874
WBVar01209875
WBVar01209876
WBVar01209877
WBVar01209878
WBVar01209879
WBVar01209880
WBVar02075326
WBVar01209881
WBVar01209882
WBVar01209883
WBVar01209884
WBVar01209885
WBVar01209886
WBVar01209887
WBVar01209888
WBVar01209889
WBVar01209890
WBVar01209891
WBVar01553024
WBVar01553025
WBVar01553026
WBVar01553027
WBVar01830892
WBVar01928527
WBVar01928528
WBVar01928529
WBVar01928530
WBVar01928531
WBVar01928532
WBVar01928533
WBVar00256252
WBVar01760372
WBVar01760373
WBVar01760374
WBVar00145281
WBVar00524821
WBVar00524822
WBVar00524823
WBVar00524824
WBVar00524825
WBVar00603693
WBVar00524826
WBVar00524827
WBVar00524828
WBVar01981684
WBVar01639804
WBVar01981685
WBVar00524829
WBVar00524830
WBVar00524831
WBVar00524832
WBVar00524833
WBVar01654899
WBVar00524834
WBVar00524835
WBVar00524836
WBVar00085443
WBVar00085444
WBVar00524837
WBVar00524838
WBVar00085445
WBVar00524839
WBVar00085446
WBVar00524840
WBVar00085447
WBVar00524841
WBVar01942185
WBVar00085448
WBVar02005543
WBVar00524842
WBVar01942186
WBVar00085449
WBVar00524843
WBVar00085450
WBVar00085451
WBVar00524844
WBVar00524845
WBVar02071482
WBVar00274747
WBVar01846004
WBVar01472618
WBVar00102021
WBVar01472619
WBVar01472621
WBVar01622277
WBVar01472622
WBVar01622278
WBVar01622279
WBVar01622280
WBVar01622281
WBVar00237415
WBVar02069091
WBVar00091556
WBVar01679682
WBVar01679683
WBVar01679684
WBVar01679685
WBVar01679686
WBVar01498960
WBVar01500067
StrainWBStrain00034914
WBStrain00005267
WBStrain00005270
WBStrain00005271
WBStrain00005272
RNASeq_FPKM (74)
GO_annotation (26)
Ortholog (37)
ParalogWBGene00007261Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013542Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020693Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00022129Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionslt-1 encodes the sole C. elegans homolog of Drosophila Split, a secreted extracellular protein containing leucine-rich and EGF-like repeats that functions as a ligand for the Robo receptor; during C. elegans larval development, slt-1 acts via the SAX-3/Robo receptor, and in parallel with UNC-6/Netrin, to direct ventral axon guidance and guidance at the midline; during embryonic development, slt-1 also functions to regulate anterior-posterior migrations of the CAN neurons; slt-1::gfp reporters are initially expressed at high levels in the anterior part of the embryo, with more moderate levels seen in dorsal tail muscles and lower levels seen in cells in the center of the body; in L1 larvae, slt-1::gfp is expressed in both dorsal and ventral muscles, with higher levels seen in dorsal muscle cells; slt-1::gfp is also expressed in a number of additional cells including some neurons, pharyngeal cells, and the anal sphincter muscle.Paper_evidenceWBPaper00004900
Curator_confirmedWBPerson1843
Date_last_updated19 Jun 2007 00:00:00
Automated_descriptionEnables signaling receptor binding activity. Involved in axon guidance; neuron migration; and regulation of neuron projection development. Predicted to be located in extracellular region. Expressed in anal sphincter muscle; anterior hypodermis; body wall musculature; nerve ring neurons; and socket cell. Human ortholog(s) of this gene implicated in atrial fibrillation; myositis (multiple); and proliferative diabetic retinopathy. Is an ortholog of human SLIT1 (slit guidance ligand 1); SLIT2 (slit guidance ligand 2); and SLIT3 (slit guidance ligand 3).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:13207Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11086)
DOID:0080745Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11086)
DOID:10223Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11086)
DOID:0060224Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11086)
Molecular_infoCorresponding_CDSF40E10.4
Corresponding_CDS_historyF40E10.4:wp90
Corresponding_transcriptF40E10.4.1
Other_sequence (11)
Associated_featureWBsf648747
WBsf648748
WBsf663583
WBsf663584
WBsf663585
WBsf717401
WBsf236701
WBsf236702
WBsf236703
Experimental_infoRNAi_resultWBRNAi00011228Inferred_automaticallyRNAi_primary
WBRNAi00086123Inferred_automaticallyRNAi_primary
WBRNAi00001158Inferred_automaticallyRNAi_primary
WBRNAi00046840Inferred_automaticallyRNAi_primary
WBRNAi00032019Inferred_automaticallyRNAi_primary
Expr_patternExpr1639
Expr8003
Expr1016319
Expr1032406
Expr1150710
Expr2015887
Expr2034120
Drives_constructWBCnstr00000844
WBCnstr00008334
WBCnstr00013053
WBCnstr00035356
WBCnstr00038306
Construct_productWBCnstr00000848
WBCnstr00000849
WBCnstr00000851
WBCnstr00000852
WBCnstr00035356
Microarray_results (20)
Expression_cluster (176)
Interaction (102)
Map_infoMapXPosition19.7628Error0.06206
PositivePositive_cloneF40E10Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4664
5528
Pseudo_map_position
Reference (74)
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