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WormBase Tree Display for Gene: WBGene00003885

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Name Class

WBGene00003885EvidenceCGC_data_submission
SMapS_parentSequenceY41G9A
IdentityVersion1
NameCGC_nameosm-5Person_evidenceWBPerson242
Sequence_nameY41G9A.1
Molecular_nameY41G9A.1
Y41G9A.1.1
CE28361
Other_nameCELE_Y41G9A.1Accession_evidenceNDBBX284606
Public_nameosm-5
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classosm
Reference_alleleWBVar00095130
Allele (145)
Legacy_informationp813 : same phenotypes as osm-1(p808) also males suicidal poor mating. ES1 ME1. NA1.
See also p813
[C.elegansII] p813 : fails to avoid 4M fructose or 4M NaCl; poor chemotaxis to NaCl; normal thermotaxis; fails to take up FITC; Daf-d; severely shortened axonemes, ectopic assembly of ciliary structures and microtubules in many sensory neurons; also males suicidal, poor mating. ES1 ME1. OA>6: m184, mn397 [Perkins et al. 1986; Starich et al. 1995; SP; DR]
[Haycraft CJ] osm-5 cloned, is Y41G9A.1 encoding homolog of murine cystic kidney disease gene Tg737. p813 is codon473stop, mn397 is G229E, sa130 is mutated at exon 3 5' donor.
StrainWBStrain00030797
WBStrain00035629
RNASeq_FPKM (74)
GO_annotation (23)
Ortholog (36)
ParalogWBGene00000244Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00003858Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00017983Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00018175Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021444Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021613Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00043992Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionosm-5 encodes the ortholog of the murine polycystic kidney disease gene Tg737 (which encodes the protein Polaris) and human IFT88; osm-5 is required for the proper morphology of the cilia of chemosensory neurons and is involved in intraflagellar transport; the abnormalities in cilia structure in osm-5 mutants lead to defects in several processes like osmotic avoidance, chemotaxis, dauer formation, male mating and life span; osm-5 is expressed in ciliated sensory neurons and localizes to the transition zones of the amphids, phasmids, labials and rays of the male tail; osm-5 expression is regulated by the RFX-type transcription factor, DAF-19, that also regulates the expression of other genes involved in cilia formation.Paper_evidenceWBPaper00004603
WBPaper00005109
Curator_confirmedWBPerson324
WBPerson567
Date_last_updated17 Jan 2012 00:00:00
Automated_descriptionPredicted to enable kinesin binding activity. Involved in several processes, including dauer entry; locomotory exploration behavior; and non-motile cilium assembly. Located in ciliary basal body; neuron projection; and non-motile cilium. Part of intraciliary transport particle B. Expressed in amphid sensillum and neurons. Used to study autosomal dominant polycystic kidney disease. Is an ortholog of human IFT88 (intraflagellar transport 88).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_infoExperimental_modelDOID:898Homo sapiensPaper_evidenceWBPaper00004603
WBPaper00004715
Accession_evidenceOMIM173900
Curator_confirmedWBPerson324
Date_last_updated30 Apr 2018 00:00:00
Disease_relevanceStudies in the worm C. elegans have contributed extensively to the finding that cystic kidney diseases can be considered ciliopathies; osm-5 is orthologous to the murine polycystic kidney disease gene Tg737, which encodes the protein Polaris and human IFT88; both polaris and OSM-5 have the tetratricopeptide repeat (TPT), a motif that mediates protein-protein interactions; the association of pathologies in mice mutant for Tg737 with ciliary defects in the kidney cells and studies in elegans that demonstrate that osm-5 is expressed and migrates within cilia, substantiate a ciliogenic role for polaris and osm-5, possibly as components of the intraflagellar transport (IFT) system; osm-5 is also required for correct ciliary targeting of lov-1 and pkd-2, genes that are orthologous to human PKD1 and PKD2, which are mutated in human autosomal dominant polycystic kidney disease.Homo sapiensPaper_evidenceWBPaper00004603
Curator_confirmedWBPerson324
Date_last_updated31 Jan 2013 00:00:00
Models_disease_in_annotationWBDOannot00000030
Models_disease_assertedWBDOannot00000513
Molecular_infoCorresponding_CDSY41G9A.1
Corresponding_transcriptY41G9A.1.1
Other_sequence (25)
Associated_feature (12)
Experimental_infoRNAi_resultWBRNAi00095205Inferred_automaticallyRNAi_primary
WBRNAi00056418Inferred_automaticallyRNAi_primary
Expr_pattern (13)
Drives_construct (12)
Construct_productWBCnstr00006237
WBCnstr00008467
WBCnstr00009069
WBCnstr00010229
WBCnstr00013368
WBCnstr00039933
AntibodyWBAntibody00000351
WBAntibody00001248
Microarray_results (19)
Expression_cluster (200)
Interaction (43)
WBProcessWBbiopr:00000001
WBbiopr:00000012
Map_infoMapXPosition-12.6622Error0.00141
Well_ordered
PositivePositive_cloneY41G9AInferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point376
377
3384
Multi_point1209
1210
1211
1212
5291
5597
Pos_neg_data3180
5450
ReferenceWBPaper00000082
WBPaper00000481
WBPaper00000608
WBPaper00000932
WBPaper00000937
WBPaper00001256
WBPaper00001399
WBPaper00001482
WBPaper00001704
WBPaper00001722
WBPaper00001786
WBPaper00001862
WBPaper00002087
WBPaper00002485
WBPaper00002967
WBPaper00003582
WBPaper00003680
WBPaper00003835
WBPaper00003954
WBPaper00004405
WBPaper00004603
WBPaper00004715
WBPaper00004854
WBPaper00005109
WBPaper00005242
WBPaper00005244
WBPaper00005274
WBPaper00005786
WBPaper00005876
WBPaper00005965
WBPaper00006166
WBPaper00006247
WBPaper00006457
WBPaper00006516
WBPaper00010640
WBPaper00010709
WBPaper00011136
WBPaper00014657
WBPaper00015209
WBPaper00016325
WBPaper00016724
WBPaper00017890
WBPaper00017999
WBPaper00018240
WBPaper00018251
WBPaper00019272
WBPaper00019340
WBPaper00024049
WBPaper00024055
WBPaper00024071
WBPaper00024175
WBPaper00024240
WBPaper00024803
WBPaper00024944
WBPaper00025051
WBPaper00025076
WBPaper00025841
WBPaper00026206
WBPaper00026601
WBPaper00026822
WBPaper00027085
WBPaper00027772
WBPaper00028082
WBPaper00028448
WBPaper00028470
WBPaper00028471
WBPaper00029013
WBPaper00029015
WBPaper00029016
WBPaper00029020
WBPaper00029029
WBPaper00029131
WBPaper00029264
WBPaper00029400
WBPaper00030735
WBPaper00030843
WBPaper00031133
WBPaper00031146
WBPaper00031170
WBPaper00031483
WBPaper00031566
WBPaper00031625
WBPaper00031632
WBPaper00031936
WBPaper00032000
WBPaper00035062
WBPaper00037836
WBPaper00038169
WBPaper00038248
WBPaper00038491
WBPaper00039675
WBPaper00040183
WBPaper00040543
WBPaper00045913
WBPaper00046926
WBPaper00055090
WBPaper00055368
WBPaper00061133
WBPaper00061444
WBPaper00062090
WBPaper00062445
WBPaper00062787
WBPaper00063946
WBPaper00064108
WBPaper00065747
RemarkSequence connection from [Haycroft CG, Thomas JH]
Data extracted from Haycraft et al (2001)
MethodGene