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WormBase Tree Display for Gene: WBGene00004046

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Name Class

WBGene00004046SMapS_parentSequenceF45E4
IdentityVersion1
NameCGC_nameplp-1Person_evidenceWBPerson539
Sequence_nameF45E4.2
Molecular_nameF45E4.2
F45E4.2.1
CE10494
Other_nameCELE_F45E4.2Accession_evidenceNDBBX284604
Public_nameplp-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classplp
Allele (21)
Legacy_information[Joel H. Rothman] Similar to the transcriptional activator pur-alpha (pur-alpha like protein)
StrainWBStrain00002953
WBStrain00032403
RNASeq_FPKM (74)
GO_annotation (19)
Ortholog (43)
ParalogWBGene00008976Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionplp-1 encodes a protein containing three PUR repeats that has similarity to the mammalian transcription factor pur alpha; plp-1 is required for embryonic development, development of the pharynx, and formation of the intestine; PLP-1 interacts with double-stranded DNA and specifically, with a Lef-1 binding site within the end-1 promoter; PLP-1 DNA binding is regulated by phosphorylation.Paper_evidenceWBPaper00006241
WBPaper00032400
Curator_confirmedWBPerson48
WBPerson1843
Date_last_updated17 Jun 2011 00:00:00
Automated_descriptionEnables double-stranded telomeric DNA binding activity. Involved in germ cell development and regulation of locomotion. Located in P granule and nucleus. Expressed in several structures, including Caa; Cpa; Psub4; oocyte; and somatic cell. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder 31. Is an ortholog of human PURB (purine rich element binding protein B).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:0070061Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9701)
Molecular_infoCorresponding_CDSF45E4.2
Corresponding_transcriptF45E4.2.1
Other_sequence (78)
Associated_featureWBsf646102
WBsf660319
WBsf978529
WBsf981787
WBsf228556
WBsf228557
WBsf228558
Gene_product_bindsWBsf038804
Transcription_factorWBTranscriptionFactor000127
Experimental_infoRNAi_result (41)
Expr_pattern (14)
Drives_constructWBCnstr00003459
WBCnstr00011658
WBCnstr00035723
WBCnstr00042523
Construct_productWBCnstr00011658
WBCnstr00035723
WBCnstr00042523
Regulate_expr_clusterWBPaper00060526:plp-1(ok2155)_downregulated
WBPaper00060526:plp-1(ok2155)_upregulated
AntibodyWBAntibody00001881
WBAntibody00002923
Microarray_results (23)
Expression_cluster (155)
Interaction (72)
Map_infoMapIVPosition3.36566Error0.000571
PositivePositive_cloneF45E4Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (15)
RemarkSequence connection from [Rothman JH]
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