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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_description (2)
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
Reference (105)
RemarkSequence connection from [Haycroft CG, Thomas JH]
Data extracted from Haycraft et al (2001)
MethodGene