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WormBase Tree Display for Gene: WBGene00002229

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Name Class

WBGene00002229SMapS_parentSequenceY43F4B
IdentityVersion1
NameCGC_nameklp-19Person_evidenceWBPerson589
Sequence_nameY43F4B.6
Molecular_nameY43F4B.6
Y43F4B.6.1
CE16631
Other_nameCELE_Y43F4B.6Accession_evidenceNDBBX284603
Public_nameklp-19
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:27WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classklp
Allele (59)
StrainWBStrain00034457
WBStrain00037513
RNASeq_FPKM (74)
GO_annotation00035665
00035666
00035667
00035668
00035669
00035670
00035671
00035672
00035673
00035674
00035675
00035676
00035677
00035678
00035679
00035680
00035681
00035682
00035683
00035684
00035685
00035686
00035687
00035688
00035689
00110234
00110235
00110236
00110237
Ortholog (41)
Paralog (19)
Structured_descriptionConcise_descriptionklp-19 encodes a plus-end-directed microtubule motor protein that is most closely related to motors of the kinesin-4 family; KLP-19 activity is essential for embryonic and larval development and is required for generating a force that aligns sister chromatid kinetochores directly opposite the spindle poles thus ensuring proper holocentric chromosome segregation; KLP-19 expression is detected in embryos and in the gonad, where it is most strongly expressed in distal mitotic nuclei and in late meiotic prophase nucleoplasm; during meiosis and mitosis, KLP-19 expression is dynamic and is detected in the nucleoplasm, the spindle body, in association with condensed chromosomes (particularly between homologous chromosomes), and in the spindle interzone.Paper_evidenceWBPaper00024405
Curator_confirmedWBPerson1843
Date_last_updated05 Jan 2005 00:00:00
Automated_descriptionPredicted to enable ATP hydrolysis activity; microtubule binding activity; and microtubule motor activity. Involved in meiotic chromosome condensation and meiotic spindle midzone assembly. Located in condensed nuclear chromosome; nucleoplasm; and spindle. Expressed in germ line. Human ortholog(s) of this gene implicated in non-syndromic X-linked intellectual disability 100. Is an ortholog of human KIF4A (kinesin family member 4A).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:0112040Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13339)
Molecular_infoCorresponding_CDSY43F4B.6
Corresponding_transcriptY43F4B.6.1
Other_sequence (18)
Associated_feature (13)
Experimental_infoRNAi_result (24)
Expr_patternExpr3116
Expr16333
Expr1011369
Expr1031306
Expr1159961
Expr2012962
Expr2031194
Drives_constructWBCnstr00042912
AntibodyWBAntibody00000778
WBAntibody00002846
WBAntibody00002919
WBAntibody00002967
WBAntibody00002973
Microarray_results (22)
Expression_cluster (173)
Interaction (34)
Map_infoMapIIIPosition21.21Error0.000801
PositivePositive_cloneY43F4BInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point5197
4549
Pseudo_map_position
Reference (17)
RemarkSequence connection from [Siddiqui SS], 02/06/11 krb.
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