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WormBase Tree Display for Gene: WBGene00002182

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Name Class

WBGene00002182SMapS_parentSequenceCHROMOSOME_III
IdentityVersion1
NameCGC_namekap-1Person_evidenceWBPerson589
Sequence_nameF08F8.3
Molecular_nameF08F8.3a
F08F8.3a.1
CE54188
F08F8.3b
CE54084
F08F8.3a.2
F08F8.3b.1
Other_nameCELE_F08F8.3Accession_evidenceNDBBX284603
Public_namekap-1
DB_infoDatabaseAceViewgene3I433
WormQTLgeneWBGene00002182
WormFluxgeneWBGene00002182
NDBlocus_tagCELE_F08F8.3
PanthergeneCAEEL|WormBase=WBGene00002182|UniProtKB=H2KZP1
familyPTHR15605
NCBIgene176041
RefSeqproteinNM_001379790.1
NM_001379791.1
TREEFAMTREEFAM_IDTF314964
TrEMBLUniProtAccG5EEE6
H2KZP1
UniProt_GCRPUniProtAccG5EEE6
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classkap
Allele (67)
Legacy_information[Siddiqui SS ]. Related to kinesin associated protein by sequence similarity.
StrainWBStrain00003712
WBStrain00031562
RNASeq_FPKM (74)
GO_annotation (19)
Ortholog (38)
Structured_descriptionConcise_descriptionkap-1 encodes a kinesin-associated protein that, along with KLP-20 and KLP-11, is part of the C. elegans heterotrimeric kinesin-II motor protein; animals homozygous for a kap-1 loss-of-function mutation have normal cilia and thus display normal dye-filling and osmotic avoidance behavior; however, animals doubly mutant for kap-1 and osm-3, which encodes a homomeric kinesin-II motor protein, do show defects in intraflagellar transport (IFT) indicating that the heteromeric kinsesin-II and homomeric OSM-3 motor protein complexes function redundantly to effect IFT; antibodies to KAP-1 detect high intensity staining in sensory neuron cilia; kap-1 expression in the AWB sensory neurons is positively regulated by FKH-2.Paper_evidenceWBPaper00003466
WBPaper00004178
WBPaper00024501
WBPaper00029400
Curator_confirmedWBPerson1843
Date_last_updated13 Oct 2008 00:00:00
Automated_descriptionContributes to microtubule motor activity. Involved in intraciliary anterograde transport; negative regulation of non-motile cilium assembly; and positive regulation of non-motile cilium assembly. Located in ciliary transition zone and non-motile cilium. Part of axonemal heterotrimeric kinesin-II complex. Expressed in ciliated neurons. Is an ortholog of human KIFAP3 (kinesin associated protein 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
Molecular_infoCorresponding_CDSF08F8.3a
F08F8.3b
Corresponding_CDS_historyF08F8.3a:wp275
F08F8.3b:wp275
Corresponding_transcriptF08F8.3a.1
F08F8.3a.2
F08F8.3b.1
Other_sequence (14)
Associated_featureWBsf645332
WBsf659176
WBsf976217
WBsf976218
WBsf976219
WBsf976220
WBsf225239
Experimental_infoRNAi_resultWBRNAi00012913Inferred_automaticallyRNAi_primary
WBRNAi00005204Inferred_automaticallyRNAi_primary
WBRNAi00044028Inferred_automaticallyRNAi_primary
Expr_pattern (14)
Drives_construct (11)
Construct_product (16)
AntibodyWBAntibody00000217
Microarray_results (21)
Expression_cluster (113)
SAGE_tagSAGE:ccaaattgatgatgagtStrandSense
Unambiguously_mapped
SAGE:ccaaattgatStrandSense
Unambiguously_mapped
SAGE:tgtcacttttcttaccaStrandSense
Unambiguously_mapped
SAGE:aaaacttggaStrandAntisense
SAGE:cattctaaaccaaatgaStrandAntisense
SAGE:attgtaataactgcacaStrandAntisense
SAGE:ggtacagttgctgagctStrandSense
Unambiguously_mapped
Interaction (29)
WBProcessWBbiopr:00000012
Map_infoMapIIIPosition-0.74971Error0.000513
PositivePositive_cloneF08F8Person_evidenceWBPerson589
Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4452
Pseudo_map_position
Reference (48)
RemarkThere are two kap-1 genes. The CGC_approved one is connected to F08F8.3a/b, the non_CGC_approved one (from the original GenBank/EMBL AF045926) is an other_name of aka-1 and is linked to D1022.7a/b/c [JAH][030120 ck1]
Map 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