Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00001374

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00001374SMapS_parentSequenceF12F3
IdentityVersion1
NameCGC_nameexp-2Person_evidenceWBPerson655
Sequence_nameF12F3.1
Molecular_name (19)
Other_nameCELE_F12F3.1Accession_evidenceNDBBX284605
Public_nameexp-2
DB_infoDatabaseAceViewgene5G623
WormQTLgeneWBGene00001374
WormFluxgeneWBGene00001374
NDBlocus_tagCELE_F12F3.1
PanthergeneCAEEL|WormBase=WBGene00001374|UniProtKB=H2KZQ6
familyPTHR11537
NCBIgene179003
RefSeqproteinNM_001380662.1
NM_001028621.5
NM_001380661.1
NM_001392526.1
TrEMBLUniProtAccQ5WRQ6
H2KZQ6
P91256
H2KZQ7
UniProt_GCRPUniProtAccH2KZQ6
OMIMgene600397
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classexp
AlleleWBVar00242463Inferred_automaticallyFrom strain object: DA1426
From strain object: JT5132
WBVar00000097Inferred_automaticallyFrom strain object: DA1426
WBVar00000090
WBVar00242464
WBVar01905311
WBVar02141083
WBVar00027136
WBVar00142627
WBVar00065145
WBVar01499528
WBVar01488673
WBVar01499173
WBVar01499174
WBVar00210085
WBVar00210087
WBVar00210088
WBVar01016433
WBVar00210089
WBVar01016434
WBVar01499740
WBVar00210090
WBVar00210091
WBVar01016435
WBVar00210092
WBVar01016436
WBVar01016437
WBVar01016438
WBVar01016439
WBVar01016440
WBVar01016441
WBVar01016442
WBVar01016443
WBVar01016444
WBVar01016445
WBVar01016446
WBVar01016447
WBVar01016448
WBVar01016449
WBVar01016450
WBVar01016451
WBVar01016452
WBVar01016453
WBVar01016454
WBVar01500129
WBVar01016455
WBVar01016456
WBVar01016457
WBVar01016458
WBVar01016459
WBVar01016460
WBVar02125146
WBVar01016461
WBVar01016462
WBVar01016463
WBVar01016464
WBVar01016465
WBVar01016466
WBVar01016467
WBVar01016468
WBVar01016469
WBVar01016470
WBVar01016471
WBVar01016472
WBVar01016473
WBVar01016474
WBVar01016475
WBVar01016476
WBVar01016477
WBVar01016478
WBVar01016479
WBVar01016480
WBVar00067869
WBVar01016481
WBVar01016482
WBVar01016483
WBVar01016484
WBVar01484149
WBVar01016485
WBVar00459848
WBVar01016486
WBVar01016487
WBVar00459849
WBVar01016488
WBVar00459850
WBVar01016489
WBVar00459851
WBVar00459852
WBVar01016490
WBVar00459853
WBVar01016491
WBVar00459854
WBVar01016492
WBVar01016493
WBVar00459855
WBVar01016494
WBVar00459856
WBVar01016495
WBVar00459857
WBVar01016496
WBVar00459858
WBVar00459859
WBVar01489130
WBVar01016497
WBVar01016498
WBVar00459860
WBVar01016499
WBVar00459861
WBVar00459862
WBVar01016500
WBVar01016501
WBVar00459863
WBVar00459864
WBVar01016502
WBVar01016503
WBVar00459865
WBVar00459866
WBVar01016504
WBVar00459867
WBVar01016505
WBVar01016506
WBVar00459868
WBVar00459869
WBVar01016507
WBVar00302186
WBVar01016508
WBVar00459870
WBVar01016509
WBVar01016510
WBVar01016511
WBVar01016512
WBVar01016513
WBVar01016514
WBVar01016515
WBVar01016516
WBVar01016517
WBVar01493018
WBVar01808239
WBVar01808240
WBVar01808241
WBVar01808242
WBVar02078592
WBVar01740432
WBVar01740433
WBVar01740434
WBVar01740435
WBVar02034580
WBVar00262019
WBVar01499496
WBVar00262022
WBVar01499316
WBVar01460147
WBVar01822080
WBVar02136451
WBVar01460148
WBVar02136452
WBVar01460150
WBVar02136453
WBVar01973721
WBVar01973722
WBVar01500066
WBVar02023741
WBVar02023742
Legacy_information[Jim Thomas] sa26/+ strongly dominant defecation and egg laying defective, expulsion muscle contraction (Exp) always absent from defecation cycle, severe egg laying defect (Egl), serotonin nonresponsive, egg laying and anal muscle normal as observed by polarized light, pumping very shallow but rapid, homozygous viable
See also sa26
[Reiner D]] Mac-d (Muscle ACtivation-Defective)
[C.elegansII] sa26sd : recessive viable; sa26/+ strongly dominant,severely constipated, jerky Unc;expulsion muscle contraction (Exp) always absent from defecation cycle, severe egg laying defect (Type A Egl), serotonin nonresponsive, egg laying and anal muscle normal as observed by polarized light, pumping very shallow but rapid. Muscle activation defective (flaccid, long). NA1 (gf).Intragenic revertants, eg sa26sa66, sa26sa68, arerecessive lethal, no dominant Exp phenotype. [Thomas 1990; JT]
StrainWBStrain00003004
WBStrain00022817
WBStrain00005574
RNASeq_FPKM (74)
GO_annotation (24)
Ortholog (44)
Paralog (13)
Structured_descriptionConcise_descriptionexp-2 encodes a member of the six-transmembrane voltage-activated (Kv-type) family of potassium channels; exp-2 is required for normal pharyngeal muscle action potentials and hence, for normal feeding behavior; in addition, exp-2 is required for chemotaxis; when expressed in Xenopus oocytes, EXP-2 displays inward rectifying currents, however when assessed in endogenous pharyngeal tissue, EXP-2 displays hyperpolarization-activated outward currents; an EXP-2 translational reporter fusion is expressed strongly in pharyngeal muscles, amphid, phasmid, and head neurons, posterior enteric muscles, and occasionally faintly in the egg-laying muscles.Paper_evidenceWBPaper00003840
WBPaper00025209
Curator_confirmedWBPerson1843
Date_last_updated22 Sep 2005 00:00:00
Automated_descriptionEnables inward rectifier potassium channel activity. Involved in potassium ion transmembrane transport. Predicted to be located in membrane. Predicted to be part of voltage-gated potassium channel complex. Expressed in intestinal cell; muscle cell; nerve ring; neurons; and pharyngeal muscle cell. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 26. Is an ortholog of human KCNF1 (potassium voltage-gated channel modifier subfamily F member 1).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:0080461Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6231)
DOID:1826Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6231)
Molecular_infoCorresponding_CDSF12F3.1a
F12F3.1b
F12F3.1c
F12F3.1d
Corresponding_CDS_historyF12F3.1:wp90
F12F3.1:wp131
Corresponding_transcript (11)
Other_sequence (27)
Associated_featureWBsf646857
WBsf1000179
WBsf1000180
WBsf1019738
WBsf1019739
WBsf231841
Experimental_infoRNAi_resultWBRNAi00044446Inferred_automaticallyRNAi_primary
WBRNAi00090201Inferred_automaticallyRNAi_primary
WBRNAi00090043Inferred_automaticallyRNAi_primary
WBRNAi00013165Inferred_automaticallyRNAi_primary
WBRNAi00089883Inferred_automaticallyRNAi_primary
WBRNAi00089832Inferred_automaticallyRNAi_primary
Expr_pattern (8)
Drives_constructWBCnstr00003504
WBCnstr00010037
WBCnstr00036984
Construct_productWBCnstr00010037
WBCnstr00022462
WBCnstr00022728
WBCnstr00036984
Microarray_results (33)
Expression_cluster (175)
Interaction (27)
WBProcessWBbiopr:00000010
Map_infoMapVPosition-0.262655Error0.010268
PositiveInside_rearradDf1059
Positive_cloneF12F3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point4436
4581
Multi_point1533
2270
3122
3550
5324
Pos_neg_data (16)
Reference (36)
MethodGene