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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
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
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