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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_nameklq-1
CELE_C25B8.1Accession_evidenceNDBBX284606
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)
Ortholog (48)
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_clusterWBPaper00035211:age-1_vs_age-1_upregulated
WBPaper00036375:enriched_in_PVD_OLL
WBPaper00037950:A-class-motor-neurons_L2-larva_expressed
WBPaper00037950:all-neurons_L2-larva_expressed
WBPaper00037950:all-neurons_larva_enriched
WBPaper00037950:all-neurons_larva_SelectivelyEnriched
WBPaper00037950:CEP-sheath-cells_Day1-adult_expressed
WBPaper00037950:glr-1(+)-neurons_L2-larva_expressed
WBPaper00037950:PVD-OLL-neurons_L3-L4-larva_expressed
WBPaper00038438:S.marcescens_24hr_downregulated_TilingArray
WBPaper00040420:ALM_PLM_enriched
WBPaper00040420:FLP_enriched
WBPaper00042215:wdr-23(tm1817)_upregulated
WBPaper00042561:smg-2(RNAi)_upregulated
WBPaper00044736:flat_dev_expression
WBPaper00045390:ubc-9(RNAi)_downregulated
WBPaper00045417:128Q-huntingtin_downreglated
WBPaper00048923:Aging_regulated
WBPaper00048988:neuron_enriched
WBPaper00048988:neuron_expressed
WBPaper00049545:jmjd-3.1(+)_upregulated
WBPaper00049736:daf-2(e1370)_upregulated_15deg-then-25deg(12hr)
WBPaper00050344:AFD-neuron_enriched
WBPaper00050344:ASER-neuron_enriched
WBPaper00050344:PLM-neuron_enriched
WBPaper00050488:adult_vs_dauer_regulated_N2_20C
WBPaper00050726:OsmoticStress_regulated_Food
WBPaper00050859:upregulated_P-granule(-)GFP(+)_vs_control_day2-adult
WBPaper00050990:NMDA-neuron_enriched
WBPaper00050990:NMDA-neuron_expressed
WBPaper00051352:Long-Term-Association-Memory_upregulated
WBPaper00051558:aging_regulated
WBPaper00053184:sma-2(rax5)_upregulated
WBPaper00053184:sma-4(rax3)_upregulated
WBPaper00053295:lin-22(icb38)_upregulated
WBPaper00053295:lin-22(ot269)_upregulated
WBPaper00053302:alovudine_24h_regulated
WBPaper00053302:stavudine_24h_regulated
WBPaper00053368:F.oxysporum_regulated
WBPaper00054758:alg-1(gk204)_upregulated
WBPaper00055137:S.maltophilia_downregulated
WBPaper00055334:DLC-1_interacting
WBPaper00055354:Metformin_upregulated
WBPaper00055354:Psora-Allantoin_upregulated
WBPaper00055354:Rapamycin-Metformin_upregulated
WBPaper00055354:Rifampicin-Allantoin_upregulated
WBPaper00055354:Rifampicin_upregulated
WBPaper00055941:nuo-6(qm200);atfs-1(gk3094)_upregulated
WBPaper00055971:nhl-2(ok818)_20C_upregulated
WBPaper00056161:hermaphrodite_enriched_siRNA
WBPaper00056284:ints-11(RNAi)_downregulated
WBPaper00056443:DietaryRestriction_upregulated
WBPaper00056443:sek-1(km4)_upregulated
WBPaper00056471:aak-1(tm1944);aak-2(ok524)_upregulated
WBPaper00056731:human-amylin_upregulated
WBPaper00058598:sin-3(tm1276)_downregulated
WBPaper00058711:paraquat_upregulated
WBPaper00058711:wdr-5(ok1417)_upregulated
WBPaper00059027:neuron-synapses_depleted
WBPaper00059224:tph-1(mg280)_upregulated
WBPaper00059471:EGL-43_interacting
WBPaper00060661:sensory-neuron_enriched
WBPaper00060811:L1_vs_adult_upregulated_neural
WBPaper00060909:atfs-1(cmh15)_downregulated
WBPaper00061203:let-418(n3536)_upregulated
WBPaper00061203:sin-3(tm1276)_upregulated
WBPaper00061203:spr-1(ok2144)_upregulated
WBPaper00061340:ADF
WBPaper00061340:ALM_PLM
WBPaper00061340:AWB
WBPaper00061340:mu_int_mu_anal
WBPaper00061340:mu_sph
WBPaper00061340:Neuroblast_ALA_RMED
WBPaper00061340:T
WBPaper00061341:28C_24h_upregulated
WBPaper00061341:28C_48h_upregulated
WBPaper00061479:hda-1(ne4752)_upregulated
WBPaper00061527:bath-38-Y105E8B.7
WBPaper00061651:DVB_enriched
WBPaper00061651:M1_enriched
WBPaper00061753:csr-1(tor159)_upregulated_25C
WBPaper00061818:ELKS-1_interacting
WBPaper00061995:mter-4(syb3662syb3403)_downregulated
WBPaper00062103:neuron_enriched
WBPaper00062146:MOG-7-degron_1h_regulated
WBPaper00062446:nhr-8(hd117)_upregulated
WBPaper00062497:xpf-1(tm2842)_upregulated
WBPaper00062585:hlh-26(ok1453)_upregulated_E.faecium
WBPaper00064088:Day-1-adult_vs_L4_downregulated_daf-16(mu86);glp-1(e2141)
WBPaper00064088:Day-1-adult_vs_L4_downregulated_fem-3(q20)
WBPaper00064088:Day-1-adult_vs_L4_downregulated_glp-1(e2141)
WBPaper00064088:Day-3-adult_vs_L4_downregulated_fem-3(q20)
WBPaper00064716:paraquat_downregulated
WBPaper00064735:bet-1(uth41)_vs_N2_upregulated
WBPaper00064735:bet-1B(OE)mys-1(RNAi)_vs_mys-1(RNAi)_downregulated
WBPaper00064735:mys-1(RNAi)_vs_N2_upregulated
WBPaper00064871:hypoxia_downregulated_F1
WBPaper00065096:25C_vs_20C_downregulated
WBPaper00065096:Day10_vs_Day1_upregulated
WBPaper00065096:npr-8(ok1439)_downregulated_Day10_20C
WBPaper00065749:Heat-Shock_upregulated_N2
WBPaper00065835:Day11_vs_Day1_upregulated
WBPaper00065835:mtH2S-AP39-D0-treatment_downregulated_Day11
WBPaper00065841:20_0
WBPaper00065841:20_2
WBPaper00065841:35_0
WBPaper00065841:35_1
WBPaper00065841:38_2
WBPaper00065841:54_0
WBPaper00065841:58_0
WBPaper00065841:58_1
WBPaper00065841:62_0
WBPaper00065841:68_1
WBPaper00065841:70_0
WBPaper00065841:95_0
WBPaper00065841:106_0
WBPaper00065841:140_0
cgc4489_group_20
WBPaper00024671:AFD_AWB_vs_unsorted_upregulated
WBPaper00025032:cluster_5
WBPaper00025141:N2_Expressed_Genes
WBPaper00026929:sir-2.1_overexpression_regulated
WBPaper00030839:Larval_Pan_Neuronal
WBPaper00030985:Enterococcus_faecalis_downregulated
WBPaper00031003:0hr_muscle_depleted
WBPaper00031003:hlh_1_enriched
WBPaper00031003:total_muscle_depleted
WBPaper00031532:Larva_Pan_Neuronal_Enriched
WBPaper00035588:alg-1(-)_upregulated
WBPaper00040210:Diazinon_24C_regulated
WBPaper00040858:eQTL_regulated_developing
WBPaper00040858:eQTL_regulated_juvenile
WBPaper00041174:environmental
WBPaper00041174:genotypic
WBPaper00041174:genotypic_and_environmental
WBPaper00041939:control_vs_EtBr-exposed_48h
WBPaper00041939:control_vs_EtBr-exposed_51h
WBPaper00041939:control_vs_UVC-EtBr-exposed_48h
WBPaper00041939:control_vs_UVC-EtBr-exposed_51h
WBPaper00041939:EtBr-exposed_vs_UVC-exposed_48h
WBPaper00041939:UVC-EtBr-exposed_vs_UVC-exposed_48h
WBPaper00041939:UVC-EtBr-exposed_vs_UVC-exposed_51h
WBPaper00041960:N2_fasting_upregulated_anytime
WBPaper00045673:colistin_upregulated
WBPaper00046548:dafachronic-acid_upregulated
WBPaper00048989:eat-2(ad465)_rapamycin_downregulated
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