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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_nameY105E8B.1a
Y105E8B.1a.1
CE28782
Y105E8B.1b
CE36223
Y105E8B.1c
CE29059
Y105E8B.1d
CE29060
Y105E8B.1e
CE31733
Y105E8B.1f
CE36224
Y105E8B.1g
CE48010
Y105E8B.1i
CE47868
Y105E8B.1j
CE48059
Y105E8B.1k
CE50243
Y105E8B.1l
CE28784
Y105E8B.1m
CE50134
Y105E8B.1n
CE50275
Y105E8B.1o
CE50292
Y105E8B.1p
CE50234
Y105E8B.1q
CE50171
Y105E8B.1r
CE50169
Y105E8B.1s
CE50164
Y105E8B.1t
CE51960
Y105E8B.1b.1
Y105E8B.1c.1
Y105E8B.1d.1
Y105E8B.1e.1
Y105E8B.1e.2
Y105E8B.1f.1
Y105E8B.1g.1
Y105E8B.1i.1
Y105E8B.1j.1
Y105E8B.1k.1
Y105E8B.1l.1
Y105E8B.1m.1
Y105E8B.1n.1
Y105E8B.1o.1
Y105E8B.1p.1
Y105E8B.1q.1
Y105E8B.1r.1
Y105E8B.1s.1
Y105E8B.1t.1
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_confirmedWBPerson1843
WBPerson1823
WBPerson567
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_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: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_feature (35)
Experimental_infoRNAi_result (31)
Expr_pattern (15)
Drives_construct (12)
Construct_productWBCnstr00010369
WBCnstr00012505
WBCnstr00016244
WBCnstr00041176
AntibodyWBAntibody00000099
WBAntibody00000422
WBAntibody00000423
WBAntibody00000472
Microarray_results (61)
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_data4782
4797
4812
4827
4842
4857
4872
4887
4902
4917
4932
4947
4962
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