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WormBase Tree Display for Gene: WBGene00002233

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Name Class

WBGene00002233SMapS_parentSequenceC25B8
IdentityVersion1
NameCGC_namekqt-1Person_evidenceWBPerson655
Sequence_nameC25B8.1
Molecular_nameC25B8.1a
C25B8.1a.1
CE27086
C25B8.1b
CE30875
C25B8.1b.1
Other_name (2)
Public_namekqt-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:27WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classkqt
Allele (129)
StrainWBStrain00036366
RNASeq_FPKM (74)
GO_annotation (21)
OrthologWBGene00051464Caenorhabditis remaneiFrom_analysisOMA
TreeFam
Inparanoid_8
WormBase-Compara
WBGene00032117Caenorhabditis briggsaeFrom_analysisOrthoMCL
OMA
Inparanoid_8
WormBase-Compara
WBGene00164558Caenorhabditis brenneriFrom_analysisOMA
TreeFam
Inparanoid_8
WormBase-Compara
WBGene00151695Caenorhabditis brenneriFrom_analysisTreeFam
WBGene00157444Caenorhabditis brenneriFrom_analysisTreeFam
WBGene00057574Caenorhabditis remaneiFrom_analysisTreeFam
WBGene00122083Caenorhabditis japonicaFrom_analysisTreeFam
WormBase-Compara
WBGene00128316Caenorhabditis japonicaFrom_analysisTreeFam
WBGene00222625Brugia malayiFrom_analysisWormBase-Compara
CBOVI.g3534Caenorhabditis bovisFrom_analysisWormBase-Compara
CSP21.g8067Caenorhabditis parvicaudaFrom_analysisWormBase-Compara
CSP26.g6802Caenorhabditis zanzibariFrom_analysisWormBase-Compara
CSP28.g17464Caenorhabditis panamensisFrom_analysisWormBase-Compara
CSP29.g2715Caenorhabditis beceiFrom_analysisWormBase-Compara
CSP31.g26464Caenorhabditis uteleiaFrom_analysisWormBase-Compara
CSP32.g297Caenorhabditis sulstoniFrom_analysisWormBase-Compara
CSP38.g18988Caenorhabditis quiockensisFrom_analysisWormBase-Compara
CSP39.g23320Caenorhabditis waitukubuliFrom_analysisWormBase-Compara
CSP40.g15687Caenorhabditis tribulationisFrom_analysisWormBase-Compara
Cang_2012_03_13_00415.g10531Caenorhabditis angariaFrom_analysisWormBase-Compara
Cni-kqt-1Caenorhabditis nigoniFrom_analysisWormBase-Compara
Csp11.Scaffold626.g6395Caenorhabditis tropicalisFrom_analysisWormBase-Compara
Csp5_scaffold_00135.g5300Caenorhabditis sinicaFrom_analysisWormBase-Compara
FL83_00321Caenorhabditis latensFrom_analysisWormBase-Compara
GCK72_024618Caenorhabditis remaneiFrom_analysisWormBase-Compara
OTIPU.nOt.2.0.1.g01299Oscheius tipulaeFrom_analysisWormBase-Compara
Sp34_X0191800Caenorhabditis inopinataFrom_analysisWormBase-Compara
chrX_pilon.g19273Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00238795Onchocerca volvulusFrom_analysisWormBase-Compara
WBGene00273190Pristionchus pacificusFrom_analysisWormBase-Compara
WBGene00259028Strongyloides rattiFrom_analysisWormBase-Compara
WBGene00292085Trichuris murisFrom_analysisWormBase-Compara
FB:FBgn0033494Drosophila melanogasterFrom_analysisEnsEMBL-Compara
Inparanoid
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
ZFIN:ZDB-GENE-090312-185Danio rerioFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
ZFIN:ZDB-GENE-090312-178Danio rerioFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
ZFIN:ZDB-GENE-070912-301Danio rerioFrom_analysisEnsEMBL-Compara
Panther
PhylomeDB
ZFIN:ZDB-GENE-080220-37Danio rerioFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
HGNC:6296Homo sapiensFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
HGNC:6297Homo sapiensFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
HGNC:6298Homo sapiensFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OMA
OrthoInspector
Panther
PhylomeDB
SonicParanoid
HGNC:6299Homo sapiensFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
MGI:1309503Mus musculusFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OMA
OrthoInspector
Panther
SonicParanoid
MGI:1926803Mus musculusFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OMA
OrthoInspector
Panther
PhylomeDB
SonicParanoid
MGI:1336181Mus musculusFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
MGI:1924937Mus musculusFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
RGD:69222Rattus norvegicusFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
RGD:621504Rattus norvegicusFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
RGD:628848Rattus norvegicusFrom_analysisEnsEMBL-Compara
Hieranoid
Inparanoid
OrthoInspector
Panther
SonicParanoid
Paralog (13)
Structured_descriptionConcise_descriptionkqt-1 encodes one of three C. elegans KCNQ-like potassium channel subunits that, with respect to humans, is most similar to the KCNQ2-5 subfamily of channel proteins; although loss of KQT-1 activity via large-scale RNAi screens results in no obvious abnormalities, KQT-1 likely functions to regulate cellular excitability as expression of KQT-1 in Xenopus oocytes can produce K+ channel currents that functionally resemble vertebrate M-currents; activity of these KQT-1 channels can be suppressed by coexpression with the human M1 muscarinic receptor and treatment with diacylglycerol analogs; a KQT-1::GFP translational fusion is expressed in pharyngeal muscle cells, in the anterior and posterior mechanosensory neurons ALM and PLM, and in some head neurons.Paper_evidenceWBPaper00004103
WBPaper00025059
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated15 Sep 2005 00:00:00
Automated_descriptionEnables potassium channel activity. Involved in G protein-coupled acetylcholine receptor signaling pathway; intracellular signal transduction; and potassium ion transport. Predicted to be located in plasma membrane and synapse. Predicted to be part of voltage-gated potassium channel complex. Expressed in head neurons; pharyngeal muscle cell; and touch receptor neurons. Used to study developmental and epileptic encephalopathy and long QT syndrome. Human ortholog(s) of this gene implicated in several diseases, including auditory system disease (multiple); autistic disorder; and electroclinical syndrome (multiple). Is an ortholog of human KCNQ4 (potassium voltage-gated channel subfamily Q member 4).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:2843Homo sapiensPaper_evidenceWBPaper00025059
Accession_evidenceOMIM192500
Curator_confirmedWBPerson324
Date_last_updated07 May 2012 00:00:00
DOID:0112202Homo sapiensPaper_evidenceWBPaper00025059
Curator_confirmedWBPerson324
Date_last_updated07 May 2012 00:00:00
Potential_modelDOID:0110558Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6298)
DOID:14264Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6296,HGNC:6297)
DOID:0080237Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6299)
DOID:10003Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6298)
DOID:12849Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6297)
DOID:0080462Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6296)
Disease_relevanceThe kqt genes in elegans (kqt-1, kqt-2, kqt-3) are most similar to the human KCNQ multi-gene family encoding potassium channels; C. elegans kqt-1 defines a subfamily of potassium channel genes along with the human KCNQ2-5 and kqt-3 is most similar to KCNQ1; mutations in human KCNQ genes have been associated with genetic disorders of cardiac arrhythmia and deafness; mutations in KCNQ2 are involved in epileptic encephalopathy (early infantile 7), Myokymia and seizures (benign neonatal 1), mutations in KCNQ3 are associated with neonatal seizures (benign neonatal 2), and those in KCNQ4 are associated with deafness (autosomal dominant 2A); studies in elegans show that the suppression of KCNQ/KQT channels by diacylglycerol (DAG) is dependent on the carboxyl terminal domains of the channel subunits and activated protein kinase C.Homo sapiensPaper_evidenceWBPaper00025059
Accession_evidenceOMIM613720
121200
Curator_confirmedWBPerson324
Date_last_updated07 May 2012 00:00:00
Models_disease_in_annotationWBDOannot00000063
WBDOannot00000301
Molecular_infoCorresponding_CDSC25B8.1a
C25B8.1b
Corresponding_transcriptC25B8.1a.1
C25B8.1b.1
Other_sequenceMJC02896_1
MJ00417
BMC10934_1
JI172162.1
JI174705.1
JI219469.1
Associated_feature (20)
Experimental_infoRNAi_resultWBRNAi00041161Inferred_automaticallyRNAi_primary
WBRNAi00001487Inferred_automaticallyRNAi_primary
WBRNAi00075817Inferred_automaticallyRNAi_primary
WBRNAi00041162Inferred_automaticallyRNAi_primary
WBRNAi00011145Inferred_automaticallyRNAi_primary
WBRNAi00041160Inferred_automaticallyRNAi_primary
Expr_patternExpr3234
Expr1018104
Expr1031310
Expr1145191
Expr2012976
Expr2031208
Drives_constructWBCnstr00011240
WBCnstr00036369
Construct_productWBCnstr00011240
WBCnstr00036369
Microarray_results (26)
Expression_cluster (146)
InteractionWBInteraction000169452
WBInteraction000173470
WBInteraction000264869
WBInteraction000301540
WBInteraction000544613
WBInteraction000578572
Map_infoMapXPosition-2.69956Error0.014064
PositivePositive_cloneC25B8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4237
Pseudo_map_position
Reference (12)
PictureWBPicture0000013535
RemarkSequence connection from [Thomas JH, Wei A]
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