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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_infoDatabaseAceViewgene5L558
WormQTLgeneWBGene00000064
SignaLinkproteinWBGene00000064
WormFluxgeneWBGene00000064
NDBlocus_tagCELE_T04C12.5
PanthergeneCAEEL|WormBase=WBGene00000064|UniProtKB=P10984
familyPTHR11937
NCBIgene179534
RefSeqproteinNM_001383398.2
KEGGKEGG_id3.6.4.-
NemaPathKEGG_id3.6.4.-
SwissProtUniProtAccP10984
UniProt_GCRPUniProtAccP10984
OMIMgene102560
102630
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:19WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classact
Allele (25)
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
ReferenceWBPaper00000608
WBPaper00000611
WBPaper00000741
WBPaper00000742
WBPaper00000785
WBPaper00000798
WBPaper00000801
WBPaper00000969
WBPaper00001090
WBPaper00001178
WBPaper00001230
WBPaper00001262
WBPaper00001401
WBPaper00001542
WBPaper00001567
WBPaper00001709
WBPaper00001895
WBPaper00001920
WBPaper00002006
WBPaper00002305
WBPaper00002748
WBPaper00004540
WBPaper00006387
WBPaper00006429
WBPaper00014087
WBPaper00014311
WBPaper00014714
WBPaper00016019
WBPaper00019693
WBPaper00024200
WBPaper00024704
WBPaper00025088
WBPaper00025227
WBPaper00027028
WBPaper00029197
WBPaper00029334
WBPaper00030672
WBPaper00031353
WBPaper00032322
WBPaper00033208
WBPaper00035956
WBPaper00038491
WBPaper00038607
WBPaper00040301
WBPaper00040903
WBPaper00044821
WBPaper00049828
WBPaper00054920
WBPaper00055090
WBPaper00057312
WBPaper00059214
WBPaper00059352
WBPaper00059799
WBPaper00060410
WBPaper00061939
WBPaper00062060
WBPaper00064107
WBPaper00064183
WBPaper00065103
WBPaper00065156
WBPaper00065589
WBPaper00066067
RemarkM03F4.2 connection removed since latter is on another chromosome. [sdm 0107]
Sequences T04C12.4 & T04C12.6 removed. email from JAH 0109
MethodGene