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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)
Interaction (72)
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