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WormBase Tree Display for Gene: WBGene00000065

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Name Class

WBGene00000065SMapS_parentSequenceT04C12
IdentityVersion1
NameCGC_nameact-3Person_evidenceWBPerson259
Sequence_nameT04C12.4
Molecular_nameT04C12.4
T04C12.4.1
CE13148
T04C12.4.2
T04C12.4.3
Other_nameact1Accession_evidenceEMBLX16796
act3Accession_evidenceEMBLX16798
CELE_T04C12.4Accession_evidenceNDBBX284605
Public_nameact-3
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:20WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classact
Allele (40)
StrainWBStrain00033516
WBStrain00005465
In_clusteract-123
RNASeq_FPKM (74)
Ortholog (46)
Paralog (11)
Structured_descriptionConcise_descriptionact-3 encodes an invertebrate actin, highly similar to ACT-1, ACT-2, and ACT-4, that functions in body wall muscle; act-3 functions with two other action isoforms, act-1 and act-2, to control cytoplasmic microfilament function in the early embryo.Paper_evidenceWBPaper00000741
WBPaper00001178
WBPaper00001709
WBPaper00014413
WBPaper00027028
Curator_confirmedWBPerson324
WBPerson567
Date_last_updated29 Mar 2007 00:00:00
Automated_descriptionExpressed in gonad and head. 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. Human ACTB Contributes to nucleosomal DNA binding activity. Human ACTB enables several functions, including Tat protein binding activity; enzyme binding activity; and kinesin binding activity. A structural constituent of postsynaptic actin cytoskeleton. Is predicted to encode a protein with the following domains: ATPase, nucleotide binding domain; Phosphorylation site; Actin; and Actin family. 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_CDST04C12.4
Corresponding_transcriptT04C12.4.1
T04C12.4.2
T04C12.4.3
Other_sequence (48)
Associated_feature (11)
Experimental_infoRNAi_result (47)
Expr_patternChronogram981
Expr4555
Expr6598
Expr14934
Expr1030026
Expr1155998
Expr2009223
Expr2027460
Drives_constructWBCnstr00002476
WBCnstr00037758
WBCnstr00041591
Construct_productWBCnstr00037758
AntibodyWBAntibody00001783
Microarray_results (48)
Expression_cluster (167)
Interaction (298)
Map_infoMapVPosition2.92811Error0.004379
PositivePositive_cloneT04C12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4140
4141
Pseudo_map_position
Reference (63)
RemarkM03F4.2 connection removed since latter is on another chromosome. [sdm 0107]
T04C12.6 connection removed. email from JAH 0109.
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene