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WormBase Tree Display for Gene: WBGene00002978

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Name Class

WBGene00002978SMapS_parentSequenceY105E8B
IdentityVersion1
NameCGC_namelev-11Person_evidenceWBPerson368
Sequence_nameY105E8B.1
Molecular_name (58)
Other_nametmy-1
Y105E8B.cCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CeTMPaper_evidenceWBPaper00005168
WBPaper00032338
CELE_Y105E8B.1Accession_evidenceNDBBX284601
Public_namelev-11
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlev
Reference_alleleWBVar00275207
Allele (206)
Legacy_informationx12 : slightly long uncoordinated mild twitcher phenotype grows well in 1 mM levamisole; strong semi-dominant suppressor of unc-90(e1463). ES3 ME2. NA3 (x1 : twitcher e1724 : lethal).
See also e1724
[Williams BD] Pat (paralysed arrest at two-fold), severe paralysis; st577 and st566 have some pharyngeal pumping.
[C.elegansII] x12 : slightly long, uncoordinated, mild twitcher phenotype; grows well in 1 mM levamisole; strong semi-dominant suppressor of unc-90(e1463). ES3 ME2. OA6: x1 (twitcher), e1724 (lethal). Also Pat (paralysed arrest at two-fold) alleles: st536 (severe paralysis),st577, st566 (some pharyngeal pumping. Greatly reduced staining for tropomyosin, probably corresponds to structural gene tmy-1. [Lewis et al. 1980; Williams and Waterston 1994; HK; ZZ]lfeLet-23 FErtility effector/regulator.PS.
[C.elegansII] Probably corresponds to lev-11. Three transcripts encoding tropomyosin, probable body wall and non-muscle isoforms (284 aa,different C-termini) and pharyngeal isoform (256 aa, different promoter). [Kagawa et al. 1995; HK]
StrainWBStrain00002959
WBStrain00033515
WBStrain00033518
WBStrain00033524
WBStrain00040917
WBStrain00040918
WBStrain00004923
RNASeq_FPKM (74)
GO_annotation (20)
Ortholog (47)
Structured_descriptionConcise_descriptionlev-11 encodes tropomyosin, an actin-binding contractile structural protein orthologous to human TROPOMYOSIN 1 (TPM1; OMIM:191010), which when mutated leads to familial hypertrophic cardiomyopathy; LEV-11 is required for embryonic development, normal body morphology, and locomotion; expressed as multiple tissue-specific isoforms generated by alternative mRNA splicing and promoter use, LEV-11 is detected in several tissues including muscle, pharynx, intestine, and the germ line.Paper_evidenceWBPaper00002748
WBPaper00004944
Curator_confirmed (3)
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables actin filament binding activity. Involved in several processes, including actin filament organization; regulation of actin polymerization or depolymerization; and spicule insertion. Located in striated muscle thin filament. Expressed in several structures, including body wall musculature; germ line; intestine; non-striated muscle; and pharynx. Human ortholog(s) of this gene implicated in intrinsic cardiomyopathy (multiple); muscle tissue disease (multiple); and thyroid gland papillary carcinoma. Is an ortholog of several human genes including TPM1 (tropomyosin 1); TPM2 (tropomyosin 2); and TPM3 (tropomyosin 3).Paper_evidenceWBPaper00065943
Curator_confirmed (2)
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:0111597Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12011)
DOID:0110926Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12012)
DOID:0110309Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12010)
DOID:0110457Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12010)
DOID:3969Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12012)
DOID:0110932Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12011)
DOID:0080326Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12010)
DOID:0080102Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12012)
DOID:2218Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12013)
Molecular_infoCorresponding_CDS (19)
Corresponding_CDS_historyY105E8B.1b:wp62
Y105E8B.1b:wp114
Y105E8B.1c:wp62
Corresponding_transcript (20)
Other_sequence (913)
Associated_featureWBsf028058
WBsf028059
WBsf028060
WBsf028061
WBsf649767
WBsf649768
WBsf663842
WBsf663843
WBsf663844
WBsf665140
WBsf665141
WBsf665142
WBsf665143
WBsf665144
WBsf665145
WBsf665146
WBsf665147
WBsf717606
WBsf986195
WBsf986196
WBsf986197
WBsf986198
WBsf986199
WBsf986200
WBsf986201
WBsf986202
WBsf1011272
WBsf1011273
WBsf1011274
WBsf1011275
WBsf1011276
WBsf220628
WBsf220629
WBsf220630
WBsf220631
Experimental_infoRNAi_result (31)
Expr_pattern (15)
Drives_construct (12)
Construct_productWBCnstr00010369
WBCnstr00012505
WBCnstr00016244
WBCnstr00041176
AntibodyWBAntibody00000099
WBAntibody00000422
WBAntibody00000423
WBAntibody00000472
Microarray_results171997_x_at
172001_x_at
175734_s_at
176396_s_at
176425_s_at
194257_x_at
A_12_P105752
A_12_P133935
A_12_P141215
A_12_P146035
A_12_P155145
GPL13394_WBGene00002978
GPL13914_Y105E8B.1
GPL14144_Y105E8B.1a_436-495_0.632_31_C
GPL14144_Y105E8B.1a_621-680_0.688_23_A
GPL14144_Y105E8B.1a_807-866_0.822_8_B
GPL19516_CGZ0041917
GPL19516_CGZ0041918
GPL19516_CGZ0041919
GPL19516_CGZ0041920
GPL19516_CGZ0041921
GPL19516_CGZ0041922
GPL19516_CGZ0041923
GPL19516_CGZ0041924
GPL19516_CGZ0041925
GPL19516_CGZ0041926
GPL19516_CGZ0041927
GPL21109_Y105E8B.1a
GPL3518_CE28782
GPL3518_CE29059
GPL3518_CE29060
GPL3518_CE31733
GPL8304_CE_WBGene00002978_A
GPL8673_Y105E8B_1aP00332
GPL8673_Y105E8B_1aP00756
GPL8673_Y105E8B_1aP00760
GPL8673_Y105E8B_1bP00059
GPL8673_Y105E8B_1bP00132
GPL8673_Y105E8B_1bP00395
GPL8673_Y105E8B_1cP00290
GPL8673_Y105E8B_1cP00319
GPL8673_Y105E8B_1cP00335
GPL8673_Y105E8B_1dP00333
GPL8673_Y105E8B_1dP00405
GPL8673_Y105E8B_1dP00665
GPL8673_Y105E8B_1eP00277
GPL8673_Y105E8B_1eP00335
GPL8673_Y105E8B_1eP00676
GPL8673_Y105E8B_1fP00117
GPL8673_Y105E8B_1fP00231
GPL8673_Y105E8B_1fP00235
GPL9450_Y105E8B.1b
GPL9450_Y105E8B.1c
GPL9450_Y105E8B.1d
GPL9450_Y105E8B.1e
cea2.3.26990
cea2.3.27003
cea2.d.06422
cea2.d.41975
cea2.d.41991
cea2.d.42009
Expression_cluster (304)
Interaction (175)
WBProcessWBbiopr:00000006
Map_infoMapIPosition25.8125Error0.018971
Well_ordered
PositivePositive_cloneY105E8BInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_data2_point209
213
214
327
5106
6076
Multi_point (11)
Pos_neg_data (13)
Reference (90)
RemarkData extracted from Williams & Waterston 1994
The gene tmy-1 was merged into this gene by krb on advice of JAH 25/02/02
MethodGene