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WormBase Tree Display for Gene: WBGene00021349

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Name Class

WBGene00021349SMapS_parentSequenceY37E3
IdentityVersion2
NameCGC_namearl-13Person_evidenceWBPerson4071
Sequence_nameY37E3.5
Molecular_name (13)
Other_nameCELE_Y37E3.5Accession_evidenceNDBBX284601
Public_namearl-13
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:04WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
220 Nov 2007 10:25:06WBPerson2970Name_changeCGC_namearl-13
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classarl
Allele (67)
StrainWBStrain00002472
WBStrain00036326
RNASeq_FPKM (74)
GO_annotation (30)
Ortholog (38)
Paralog (14)
Structured_descriptionConcise_descriptionarl-13 encodes the ortholog of human Arl13b which encodes the small ciliary G protein, adenosine diphosphate ribosylation factor-like protein; arl-13 is required for normal ciliary morphology and function and intraflagellar transport (IFT), arl-13 functions with the small GTPase, arl-3 for the stability of the IFT complex; arl-13 also interacts genetically with IFT-related genes like nphp-4, klp-11, bbs-8 and dyf-5 to maintain ciliary structure and anterograde IFT; ARL-13 is expressed in ciliated sensory neurons in the proximal ciliary regions and associates with the ciliary membrane via palmitoyl anchors.Curator_confirmedWBPerson324
Date_last_updated26 Jan 2012 00:00:00
Automated_descriptionPredicted to enable GTP binding activity and GTPase activity. Involved in cilium organization; receptor localization to non-motile cilium; and sensory perception of chemical stimulus. Acts upstream of or within motile cilium assembly. Located in plasma membrane bounded cell projection. Expressed in ciliated neurons and head. Used to study Joubert syndrome. Human ortholog(s) of this gene implicated in Joubert syndrome 8. Is an ortholog of human ARL13B (ADP ribosylation factor like GTPase 13B).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:0050777Homo sapiensPaper_evidenceWBPaper00036031
WBPaper00036362
Curator_confirmedWBPerson324
WBPerson38202
Date_last_updated03 Jul 2018 00:00:00
Potential_modelDOID:0111003Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:25419)
Models_disease_assertedWBDOannot00000034
WBDOannot00000602
WBDOannot00000603
Molecular_infoCorresponding_CDSY37E3.5a
Y37E3.5b
Y37E3.5c
Y37E3.5d
Corresponding_CDS_historyY37E3.5:wp147
Corresponding_transcriptY37E3.5a.1
Y37E3.5b.1
Y37E3.5c.1
Y37E3.5c.2
Y37E3.5d.1
Other_sequenceJI255318.1
Associated_featureWBsf034252
WBsf047494
WBsf643078
WBsf982802
WBsf1009288
WBsf217272
Experimental_infoRNAi_resultWBRNAi00055938Inferred_automaticallyRNAi_primary
Expr_pattern (15)
Drives_construct (34)
Construct_product (14)
Microarray_results (21)
Expression_cluster (130)
Interaction (26)
Map_infoMapIPosition-12.0683Error0.035686
PositivePositive_cloneY37E3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (28)
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