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WormBase Tree Display for Gene: WBGene00021461

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Name Class

WBGene00021461SMapS_parentSequenceY39G10AR
IdentityVersion3
NameCGC_namenekl-1Person_evidenceWBPerson353
Sequence_nameY39G10AR.3
Molecular_nameY39G10AR.3a
Y39G10AR.3a.1
CE49798
Y39G10AR.3b
CE49838
Y39G10AR.3b.1
Y39G10AR.3c
Y39G10AR.3d
Other_nameCELE_Y39G10AR.3Accession_evidenceNDBBX284601
Public_namenekl-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:04WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
229 Nov 2004 15:34:28WBPerson2970EventAcquires_mergeWBGene00021462
316 Feb 2007 14:39:36WBPerson2970Name_changeCGC_namenekl-1
Acquires_mergeWBGene00021462
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnekl
Allele (387)
StrainWBStrain00032153
WBStrain00052052
WBStrain00052053
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (37)
ParalogWBGene00017033Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00017578Caenorhabditis elegansFrom_analysisPanther
WBGene00022631Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00008956Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013694Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020324Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable protein serine/threonine kinase activity. Predicted to be involved in phosphorylation. Predicted to be located in nucleus. Expressed in amphid neurons and lumbar neurons. Human ortholog(s) of this gene implicated in lethal congenital contracture syndrome; nephronophthisis 9; and renal-hepatic-pancreatic dysplasia. Is an ortholog of human NEK9 (NIMA related kinase 9).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:0060558Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18591)
DOID:0111120Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13387)
DOID:0060259Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13387)
Molecular_infoCorresponding_CDSY39G10AR.3a
Y39G10AR.3b
Corresponding_CDS_historyY39G10AR.3:wp124
Y39G10AR.3:wp127
Y39G10AR.3:wp243
Corresponding_transcriptY39G10AR.3c
Y39G10AR.3d
Y39G10AR.3a.1
Y39G10AR.3b.1
Other_sequence (12)
Associated_feature (14)
Experimental_infoRNAi_resultWBRNAi00004597Inferred_automaticallyRNAi_primary
WBRNAi00056276Inferred_automaticallyRNAi_primary
WBRNAi00056277Inferred_automaticallyRNAi_primary
Expr_patternExpr12765
Expr1025642
Expr1039376
Expr1159759
Expr2013952
Expr2032191
Drives_constructWBCnstr00022797
Microarray_results (28)
Expression_cluster (132)
Map_infoMapIPosition-8.92543Error0.029913
PositivePositive_cloneY39G10ARInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027258
WBPaper00031387
WBPaper00038491
WBPaper00049300
WBPaper00055090
WBPaper00061306
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