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WormBase Tree Display for Gene: WBGene00006792

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Name Class

WBGene00006792SMapS_parentSequenceT06H11
IdentityVersion3
NameCGC_nameunc-58Person_evidenceWBPerson261
Sequence_nameT06H11.1
Molecular_name (21)
Other_nametwk-18CGC_data_submission
CELE_T06H11.1Accession_evidenceNDBBX284606
Public_nameunc-58
DB_infoDatabaseAceViewgeneXK722
WormQTLgeneWBGene00006792
WormFluxgeneWBGene00006792
NDBlocus_tagCELE_T06H11.1
PanthergeneCAEEL|WormBase=WBGene00006792|UniProtKB=Q22271
familyPTHR11003
NCBIgene181224
RefSeqproteinNM_171758.5
NM_001373460.3
NM_001373459.2
NM_001373458.4
NM_001373457.2
NM_001373456.2
NM_171759.6
SwissProtUniProtAccQ22271
TrEMBLUniProtAccA0A4V0IKI8
A0A4V0IL39
A0A4V0IKM3
A0A4V0INP7
A0A4V0INX3
UniProt_GCRPUniProtAccQ22271
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:43WBPerson1971EventImportedInitial conversion from geneace
220 May 2019 15:21:47WBPerson4025EventAcquires_mergeWBGene00011553
320 May 2019 15:21:47WBPerson4025EventAcquires_mergeWBGene00011552
Acquires_mergeWBGene00011553
WBGene00011552
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00143382
Allele (568)
Legacy_informatione665dm : `shaker' : animals short rigidly paralysed with constant shaking of body; e665/+ phenotype similar but weaker animals slightly longer and less rigid. ES3 ME0. NA (dominant) 5 (e415 n495 (similar phenotype) e778 (weaker phenotype)). Dominant alleles revert intragenically e.g. e665e2112 : recessive weak Unc (probable null phenotype).
See also e415, e665, e757, e778, e1320, e2112, n272, n276, n278, n284, n286, n288, n495, n1273
[Reiner D]] Mac-h (Hyper-ACtivate Muscle)
[C.elegansII] e665dm : `shaker', animals short, rigidly paralysed with constant shaking of body; e665/+ phenotype similar but weaker, animals slightly longer and less rigid. Muscle hyperactivated, sticky pumping, short.ES3 ME0. OA4 (dominant): e415, n495 (similar), e778 (weaker phenotype), etc. Dominant alleles revert intragenically e.g. e665e2112 : recessive weak Unc (probable null phenotype). [Brenner 1974; Park and Horvitz 1986; JT]
StrainWBStrain00026762
WBStrain00026763
WBStrain00026792
WBStrain00027002
WBStrain00004431
WBStrain00004508
WBStrain00004193
WBStrain00006242
WBStrain00055081
WBStrain00054759
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (35)
Paralog (47)
Structured_descriptionConcise_descriptionunc-58 encodes one of 44 C. elegans TWK (two-P domain K+) potassium channel subunits that contain two pore-forming domains and four transmembrane domains; unc-58 was originally defined by gain-of-function (gf) mutations that result in paralysis and a shortened (dumpy) body morphology due to hypercontraction of body wall muscle; unc-58 gf mutations also result in constitutive egg-laying; as loss of UNC-58 function via reversion or RNA-mediated interference (RNAi) results in either no abnormalities or only a weakly uncoordinated phenotype, UNC-58 likely functions redudantly with other TWK channels to regulate locomotion and egg-laying; UNC-58 is expressed in motor neurons and interneurons.Paper_evidenceWBPaper00002305
WBPaper00002665
WBPaper00004644
WBPaper00005654
WBPaper00017138
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables outward rectifier potassium channel activity. Involved in several processes, including muscle contraction; parturition; and regulation of muscle contraction. Predicted to be located in membrane. Expressed in interneuron and motor neurons. Is an ortholog of human KCNK17 (potassium two pore domain channel subfamily K member 17) and KCNK5 (potassium two pore domain channel subfamily K member 5).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_CDST06H11.1a
T06H11.1b
T06H11.1c
T06H11.1d
T06H11.1e
T06H11.1f
T06H11.1g
Corresponding_CDS_historyT06H11.1:wp83
Corresponding_transcriptT06H11.1a.1
T06H11.1b.1
T06H11.1c.1
T06H11.1d.1
T06H11.1e.1
T06H11.1f.1
T06H11.1g.1
Other_sequence (29)
Associated_feature (17)
Experimental_info (7)
Map_infoMapXPosition1.75032Error0.007954
Well_ordered
PositiveInside_rearrstDp2
nDf19
Positive_cloneT06H11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point (15)
Multi_point442
551
651
791
792
1343
2260
2454
4314
4494
Pos_neg_data272
497
942
656
661
ReferenceWBPaper00000031
WBPaper00000565
WBPaper00000608
WBPaper00000914
WBPaper00001709
WBPaper00002305
WBPaper00002485
WBPaper00004376
WBPaper00005927
WBPaper00006103
WBPaper00013889
WBPaper00014961
WBPaper00015071
WBPaper00016043
WBPaper00016713
WBPaper00017024
WBPaper00017174
WBPaper00017414
WBPaper00017685
WBPaper00021740
WBPaper00022012
WBPaper00022642
WBPaper00023739
WBPaper00023964
WBPaper00026748
WBPaper00027237
WBPaper00027249
WBPaper00028462
WBPaper00029020
WBPaper00038491
WBPaper00038946
WBPaper00040284
WBPaper00041300
WBPaper00048092
WBPaper00052540
WBPaper00052822
WBPaper00055090
WBPaper00056919
WBPaper00059990
WBPaper00062373
WBPaper00064001
WBPaper00064887
WBPaper00065105
RemarkThe other-name twk-18 is different from the CGC-approved main name twk-18 (C24A3.6)CGC_data_submission
MethodGene