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WormBase Tree Display for Gene: WBGene00000064

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Name Class

WBGene00000064SMapS_parentSequenceT04C12
IdentityVersion1
NameCGC_nameact-2Person_evidenceWBPerson259
Sequence_nameT04C12.5
Molecular_nameT04C12.5
T04C12.5.1
CE13150
Other_nameact2Accession_evidenceEMBLX16797
CELE_T04C12.5Accession_evidenceNDBBX284605
Public_nameact-2
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:19WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classact
AlleleWBVar00000016Inferred_automaticallyFrom strain object: DA468
WBVar00092478Inferred_automaticallyFrom strain object: EU1383
From strain object: RB1180
WBVar00094711
WBVar00094749
WBVar01499929
WBVar01499930
WBVar00469962
WBVar00469963
WBVar00469964
WBVar01499645
WBVar01500208
WBVar01500209
WBVar01046549
WBVar01046550
WBVar01046551
WBVar01046552
WBVar01046553
WBVar01046554
WBVar01499299
WBVar01046555
WBVar01046556
WBVar01046557
WBVar01046558
WBVar01046559
WBVar01499316
StrainWBStrain00031881
WBStrain00005465
WBStrain00007342
WBStrain00007350
WBStrain00007351
WBStrain00007357
WBStrain00007359
In_clusteract-123
RNASeq_FPKM (74)
GO_annotation (21)
Ortholog (57)
Paralog (11)
Structured_descriptionConcise_descriptionact-2 encodes one of five C. elegans actins; act-2 functions redundantly in early embryonic cortical microfilaments with act-1 and act-3, and dominant mutations in act-2 result in uncoordinated locomotion; an ACT-2::GFP reporter fusion is expressed in the cytoplasm of embryonic cells and is also found in contractile filaments in adult muscle cells.Paper_evidenceWBPaper00001178
WBPaper00001709
WBPaper00027028
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated29 May 2013 00:00:00
Automated_descriptionPredicted to enable ATP binding activity. Involved in several processes, including cortical actin cytoskeleton organization; cytoskeleton-dependent cytokinesis; and embryo development. Located in actin filament and cell cortex. Expressed in body wall musculature; gonad; hypodermis; and neurons. Human ortholog(s) of this gene implicated in several diseases, including Baraitser-Winter syndrome 1; Baraitser-Winter syndrome 2; and autosomal dominant nonsyndromic deafness 20. Is an ortholog of human ACTB (actin beta).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:1588Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:132)
DOID:0081113Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:144)
DOID:10881Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:132)
DOID:0081112Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:132)
DOID:0110550Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:144)
Molecular_infoCorresponding_CDST04C12.5
Corresponding_transcriptT04C12.5.1
Other_sequence (476)
Associated_feature (16)
Experimental_infoRNAi_result (49)
Expr_patternExpr3813
Expr4555
Expr1030025
Expr1155999
Expr2009222
Expr2027459
Drives_constructWBCnstr00011672
WBCnstr00016094
WBCnstr00037759
Construct_productWBCnstr00011672
WBCnstr00016094
WBCnstr00037759
AntibodyWBAntibody00001783
Microarray_results (23)
Expression_cluster (206)
Interaction (415)
WBProcessWBbiopr:00000096
Map_infoMapVPosition2.94351Error0.003498
PositivePositive_cloneT04C12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point6177
6203
Multi_point4140
4141
Reference (62)
RemarkM03F4.2 connection removed since latter is on another chromosome. [sdm 0107]
Sequences T04C12.4 & T04C12.6 removed. email from JAH 0109
MethodGene