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WormBase Tree Display for Gene: WBGene00006587

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Name Class

WBGene00006587SMapS_parentSequenceF53A9
IdentityVersion1
NameCGC_nametnt-2Person_evidenceWBPerson819
Sequence_nameF53A9.10
Molecular_nameF53A9.10
F53A9.10.1
CE34313
Other_nameCELE_F53A9.10Accession_evidenceNDBBX284606
Public_nametnt-2
DB_infoDatabaseAceViewgeneXJ340
WormQTLgeneWBGene00006587
WormFluxgeneWBGene00006587
NDBlocus_tagCELE_F53A9.10
PanthergeneCAEEL|WormBase=WBGene00006587|UniProtKB=Q7Z072
familyPTHR11521
NCBIgene181119
RefSeqproteinNM_001029532.4
TrEMBLUniProtAccQ7Z072
UniProt_GCRPUniProtAccQ7Z072
OMIMgene191041
191045
600692
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:41WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtnt
Allele (38)
StrainWBStrain00035798
RNASeq_FPKM (74)
GO_annotation00082952
00082953
00082954
00082955
00114388
00114389
Ortholog (54)
ParalogWBGene00003495Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00006589Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006588Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable tropomyosin binding activity. Predicted to be involved in muscle contraction and sarcomere organization. Predicted to be part of troponin complex. Human ortholog(s) of this gene implicated in several diseases, including distal arthrogryposis type 2B2; intrinsic cardiomyopathy (multiple); and nemaline myopathy (multiple). Is an ortholog of human TNNT1 (troponin T1, slow skeletal type); TNNT2 (troponin T2, cardiac type); and TNNT3 (troponin T3, fast skeletal type).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_model (14)
Molecular_infoCorresponding_CDSF53A9.10
Corresponding_CDS_historyF53A9.10:wp102
F53A9.10b:wp275
Corresponding_transcriptF53A9.10.1
Other_sequence (614)
Associated_featureWBsf654230
WBsf655689
WBsf655690
WBsf1006224
WBsf1023453
WBsf237702
WBsf237703
WBsf237704
Experimental_infoRNAi_result (17)
Expr_patternChronogram1633
Expr6144
Expr1022341
Expr1032720
Expr1151870
Expr2017435
Expr2035574
Drives_constructWBCnstr00003316
WBCnstr00034286
Construct_productWBCnstr00034286
Microarray_results (30)
Expression_cluster (229)
Interaction (65)
Map_infoMapXPosition0.293773Error0.032461
PositivePositive_cloneF53A9Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4729
Pseudo_map_position
ReferenceWBPaper00027020
WBPaper00027740
WBPaper00028374
WBPaper00035956
WBPaper00038491
WBPaper00055090
WBPaper00057383
RemarkSequence connection from [Bucher EA]. 02/06/12 krb.
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene