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WormBase Tree Display for Gene: WBGene00006318

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Name Class

WBGene00006318EvidencePerson_evidenceWBPerson655
SMapS_parentSequenceF34D6
IdentityVersion1
NameCGC_namesup-9Person_evidenceWBPerson261
Sequence_nameF34D6.3
Molecular_nameF34D6.3
F34D6.3.1
CE28297
Other_nametwk-23Person_evidenceWBPerson655
twk-38Person_evidenceWBPerson655
CELE_F34D6.3Accession_evidenceNDBBX284602
Public_namesup-9
DB_infoDatabaseAceViewgene2C976
WormQTLgeneWBGene00006318
WormFluxgeneWBGene00006318
NDBlocus_tagCELE_F34D6.3
PanthergeneCAEEL|WormBase=WBGene00006318|UniProtKB=O17185
familyPTHR11003
NCBIgene173613
RefSeqproteinNM_061932.6
SwissProtUniProtAccO17185
UniProt_GCRPUniProtAccO17185
OMIMgene603220
605874
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:40WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsup
AlleleWBVar00090167Inferred_automaticallyFrom strain object: MT3589
WBVar00090131Inferred_automaticallyFrom strain object: MT5920
WBVar00089641
WBVar02147477
WBVar00090414
WBVar00088516
WBVar00089443
WBVar00089310
WBVar00089567
WBVar00090411
WBVar00088517
WBVar00089633
WBVar00089571
WBVar02147479
WBVar00090211
WBVar00089340
WBVar00089346
WBVar00089440
WBVar02147478
WBVar00090160
WBVar00089355
WBVar00090296
WBVar00089377
WBVar00241304
WBVar00089572
WBVar00089639
WBVar00089376
WBVar00089884
WBVar00089887
WBVar01499702
WBVar00089891
WBVar00089895
WBVar00089898
WBVar00089900
WBVar00089901
WBVar00089903
WBVar00089911
WBVar02056920
WBVar00090367
WBVar01898487
WBVar02056921
WBVar00090368
WBVar02056922
WBVar00090369
WBVar00089302
WBVar01825432
WBVar00089308
WBVar00089311
WBVar00089312
WBVar00089313
WBVar00089331
WBVar00546980
WBVar00089337
WBVar00089341
WBVar00546981
WBVar00546985
WBVar00089350
WBVar00089357
WBVar00546988
WBVar00089358
WBVar00546990
WBVar00089380
WBVar00089382
WBVar00089387
WBVar00089397
WBVar00359881
WBVar01695040
WBVar01500106
WBVar00100621
WBVar00090405
WBVar00090406
WBVar00089436
WBVar00090407
WBVar00090408
WBVar00090409
WBVar00090410
WBVar00090412
WBVar00090413
WBVar00090415
WBVar00090417
WBVar00603996
WBVar00090418
WBVar00167588
WBVar00167589
WBVar00090419
WBVar01790435
WBVar02086245
WBVar00167590
WBVar00090420
WBVar00167591
WBVar00167592
WBVar00167593
WBVar00088506
WBVar00090429
WBVar00167594
WBVar00088507
WBVar01959508
WBVar00090430
WBVar00167595
WBVar00088508
WBVar01477133
WBVar00090431
WBVar00167596
WBVar00088509
WBVar00090432
WBVar00090679
WBVar00167597
WBVar00088510
WBVar00090433
WBVar00167598
WBVar00167599
WBVar00090434
WBVar00088511
WBVar00090435
WBVar00167600
WBVar00090165
WBVar00088512
WBVar00088513
WBVar00090436
WBVar00088514
WBVar00090437
WBVar00090438
WBVar00088515
WBVar00090439
WBVar00090440
WBVar00090441
WBVar00090442
WBVar00090443
WBVar00090444
WBVar00090445
WBVar00090179
WBVar00090180
WBVar00089562
WBVar01625897
WBVar00090209
WBVar01718718
WBVar00090210
WBVar01718719
WBVar00090212
WBVar00090213
WBVar01536532
WBVar00144901
WBVar00144903
WBVar02080778
WBVar00713737
WBVar02080779
WBVar00713738
WBVar02080780
WBVar00713739
WBVar00089648
WBVar00089656
WBVar00713740
WBVar00713741
WBVar00713742
WBVar00713743
WBVar01764986
WBVar00713744
WBVar01764987
WBVar00713745
WBVar01364678
WBVar00713746
WBVar00713747
WBVar00713748
WBVar00713749
WBVar00713750
WBVar00713751
WBVar00713752
WBVar00713753
WBVar00713754
WBVar00713755
WBVar02150244
WBVar00713756
WBVar01364726
WBVar00713757
WBVar01364728
WBVar01364732
WBVar00713758
WBVar01850968
WBVar00713759
WBVar01364733
WBVar00713760
WBVar01850969
WBVar01850970
WBVar01364739
WBVar00713761
WBVar00713762
WBVar01850971
WBVar01364740
WBVar00713763
WBVar01233579
WBVar01233580
WBVar00090295
WBVar01915847
WBVar01915849
WBVar01915850
WBVar01242617
WBVar01503547
WBVar01503548
WBVar01503549
WBVar01503550
WBVar01503551
WBVar01503552
WBVar01503553
WBVar01503554
WBVar01503555
WBVar01503556
WBVar01503557
WBVar01503558
WBVar01503559
WBVar01503560
Legacy_informationn180 : recessive suppressor of unc-93(e1500) no phenotype alone; probably null allele. ES3 in presence of e1500 ME3. NA > 20 (n180spo n192uvi etc.; all resemble n180).
See also n180, n186, n188, n189, n190, n191, n222, n223, n229, n233, n238, n241, n260, n261, n264, n266, n271, n345, n350, n353, n508, n514, n518, n519, n625, n634, n636, n659, n668, n1009, n1012, n1016, n1020, n1023, n1025, n1026, n1028, n1037, n1330
[Reiner D]] Mac-d (Muscle ACtivation-Defective)
[C.elegansII] n180 : recessive suppressor of unc-93(e1500) no phenotype alone; probably null allele. ES3 in presence of e1500 ME3. OA>20(lf):n180spo, n192uvi, n186, n350 (all resemble n180). Also neomorphic dominant allele n1550sd(severe rubber-band, almost sterile, inviable;n1550/+ strong "rubber-band" Unc-93 phenotype. Muscle activation defective (flaccid, long)). Also dominant negative suppressor alleles n1435, n242 (semidominant suppressors of sup-10(n983). [Greenwald and Horvitz 1980, Levin & Horvitz 1993]
Strain (11)
RNASeq_FPKM (74)
GO_annotation (21)
Ortholog (38)
Paralog (47)
Structured_descriptionConcise_descriptionsup-9 encodes one of 44 C. elegans TWK (two-P domain K+) potassium channel subunits that contain two pore-forming domains and four transmembrane domains; sup-9 was originally defined by gain-of-function mutations that result in defects in pharyngeal, body-wall, egg-laying, and enteric muscle activation; loss of sup-9 function via reversion or RNA-mediated interference (RNAi) does not result in any abnormalities suggesting that SUP-9 may function redundantly with other TWK channels; SUP-9 is expressed in neurons and muscle.Paper_evidenceWBPaper00002305
WBPaper00004644
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable outward rectifier potassium channel activity and potassium ion leak channel activity. Involved in regulation of muscle contraction. Located in muscle cell projection membrane and striated muscle dense body. Expressed in body wall musculature; muscle cell; and neurons. Human ortholog(s) of this gene implicated in Birk-Barel syndrome and primary pulmonary hypertension. Is an ortholog of human KCNK3 (potassium two pore domain channel subfamily K member 3) and KCNK9 (potassium two pore domain channel subfamily K member 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:14557Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6278)
DOID:0050675Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6283)
Molecular_infoCorresponding_CDSF34D6.3
Corresponding_transcriptF34D6.3.1
Other_sequence (14)
Associated_featureWBsf649937
WBsf987013
WBsf1011749
WBsf222784
Experimental_infoRNAi_result (6)
Expr_patternExpr1378
Expr2772
Expr2775
Expr2776
Expr2777
Expr1010241
Expr1032552
Expr1150142
Expr2017133
Expr2035269
Drives_constructWBCnstr00000319
WBCnstr00034398
Construct_productWBCnstr00034398
AntibodyWBAntibody00000681
Microarray_results (18)
Expression_cluster (114)
Interaction (50)
Map_infoMapIIPosition-12.1433Error0.015949
Well_ordered
PositiveInside_rearrnDf2
nDf3
nDf4
nDf5
Positive_cloneF34D6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point404
784
6131
7115
Multi_point (12)
Pos_neg_data454
458
460
462
Landmark_gene
Reference (57)
MethodGene