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WormBase Tree Display for Gene: WBGene00003495

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Name Class

WBGene00003495SMapS_parentSequenceT22E5
IdentityVersion1
NameCGC_namemup-2Person_evidenceWBPerson1052
Sequence_nameT22E5.5
Molecular_nameT22E5.5
T22E5.5.1
CE04994
Other_nametnt-1
CELE_T22E5.5Accession_evidenceNDBBX284606
Public_namemup-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmup
Allele (28)
Legacy_information[C.elegansII] e2346ts : embryonic temp-shift leads to lethal mispositioning and deformity of body-wall muscle; larval temp-shift leads to sterility, defects in oviduct muscle. OA1: up1 (non-conditional, lethal with arrest as kinked larva; probable null, nonsense mutation). Cloned: encodes troponin T homolog. [EE; UG]
StrainWBStrain00006650
WBStrain00006651
WBStrain00006652
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (36)
ParalogWBGene00006587Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00006589Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006588Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionmup-2 encodes the muscle contractile protein troponin T ( TnT ) homologous to vertebrate and invertebrate TnT and contains an invertebrate- specific COOH -terminal tail; mup-2 affects embryonic body wall muscle cell contraction, sarcomere organization, cell positioning, regulated muscle contraction in larval and adult body wall muscle, epidermal morphogenesis, and is required for proper function of the hermaphrodite nonstriated oviduct myoepithelial sheath, proper growth, and fertility.Paper_evidenceWBPaper00002414
WBPaper00003294
WBPaper00006395
Curator_confirmedWBPerson48
Date_last_updated11 Mar 2005 00:00:00
Automated_descriptionPredicted to enable tropomyosin binding activity. Involved in several processes, including axonal fasciculation; muscle structure development; and ovulation. 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_CDST22E5.5
Corresponding_transcriptT22E5.5.1
Other_sequence (140)
Associated_featureWBsf654064
WBsf670625
WBsf670626
WBsf1005570
WBsf1005571
WBsf1023097
WBsf237478
WBsf237479
WBsf237480
Experimental_infoRNAi_result (21)
Expr_patternExpr1026876
Expr1031599
Expr1157386
Expr2013825
Expr2032065
Drives_constructWBCnstr00036087
Construct_productWBCnstr00036087
Microarray_results (23)
Expression_cluster (248)
InteractionWBInteraction000000340
WBInteraction000000746
WBInteraction000000747
WBInteraction000009834
WBInteraction000028544
WBInteraction000031314
WBInteraction000114225
WBInteraction000117611
WBInteraction000117612
WBInteraction000117613
WBInteraction000117616
WBInteraction000120960
WBInteraction000135573
WBInteraction000137984
WBInteraction000140885
WBInteraction000151660
WBInteraction000165757
WBInteraction000166173
WBInteraction000166387
WBInteraction000167116
WBInteraction000169132
WBInteraction000169501
WBInteraction000169536
WBInteraction000169691
WBInteraction000173640
WBInteraction000196144
WBInteraction000238209
WBInteraction000249305
WBInteraction000266232
WBInteraction000279674
WBInteraction000286502
WBInteraction000316513
WBInteraction000324669
WBInteraction000342566
WBInteraction000343630
WBInteraction000370585
WBInteraction000374673
WBInteraction000381882
WBInteraction000387176
WBInteraction000387878
WBInteraction000387948
WBInteraction000388318
WBInteraction000412535
WBInteraction000417034
WBInteraction000421325
WBInteraction000443836
WBInteraction000448562
WBInteraction000449889
WBInteraction000451042
WBInteraction000462134
WBInteraction000538819
WBInteraction000539911
WBInteraction000550969
WBInteraction000552299
WBInteraction000552487
WBInteraction000553354
WBInteraction000553639
WBInteraction000554944
WBInteraction000554945
WBInteraction000554946
WBInteraction000559492
WBInteraction000561697
WBInteraction000562294
WBInteraction000562333
WBInteraction000564074
WBInteraction000566247
WBInteraction000566526
WBInteraction000569414
WBInteraction000572159
WBInteraction000572780
WBInteraction000576604
WBInteraction000580190
WBProcessWBbiopr:00000006
WBbiopr:00000067
Map_infoMapXPosition-2.91797Error0.002167
Well_ordered
PositivePositive_cloneR04A4
T22E5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point3386
3694
3958
Reference (39)
MethodGene