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WormBase Tree Display for Gene: WBGene00019424

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Name Class

WBGene00019424SMapS_parentSequenceK06A1
IdentityVersion2
NameCGC_nameaptf-1Person_evidenceWBPerson1997
Sequence_nameK06A1.1
Molecular_nameK06A1.1
K06A1.1.1
CE35990
Other_nameCELE_K06A1.1Accession_evidenceNDBBX284602
Public_nameaptf-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:01WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
218 Apr 2008 09:32:24WBPerson2970Name_changeCGC_nameaptf-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classaptf
Allele (16)
StrainWBStrain00036781
WBStrain00008308
WBStrain00008309
WBStrain00008310
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (52)
ParalogWBGene00009202Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00009203Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00013383Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionaptf-1 encodes one of four C. elegans AP-2-like transcription factors; APTF-1 activity is required in the RIS interneuron for sleep-like quiescence induced by neuropeptide signaling; aptf-1 is expressed in five head interneurons.Paper_evidenceWBPaper00044407
Curator_confirmedWBPerson1843
Date_last_updated24 Mar 2014 00:00:00
Automated_descriptionPredicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II and sleep. Predicted to be located in nucleus. Expressed in head neurons and pharyngeal neurons. Human ortholog(s) of this gene implicated in Char syndrome; branchiooculofacial syndrome; and dilated cardiomyopathy. Is an ortholog of human TFAP2C (transcription factor AP-2 gamma).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:0050691Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11742)
DOID:12930Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11742)
DOID:0060563Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11743)
DOID:13832Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11743)
Molecular_infoCorresponding_CDSK06A1.1
Corresponding_CDS_historyK06A1.1:wp112
Corresponding_transcriptK06A1.1.1
Other_sequence (18)
Associated_featureWBsf978621
WBsf988169
WBsf221447
WBsf221448
WBsf221449
Transcription_factorWBTranscriptionFactor000240
Experimental_infoRNAi_resultWBRNAi00033998Inferred_automaticallyRNAi_primary
WBRNAi00050014Inferred_automaticallyRNAi_primary
WBRNAi00022394Inferred_automaticallyRNAi_primary
Expr_patternExpr7607
Expr11364
Expr1018338
Expr1153707
Expr2009370
Expr2027606
Drives_constructWBCnstr00012752
WBCnstr00018465
WBCnstr00018466
WBCnstr00018469
WBCnstr00018492
WBCnstr00022594
WBCnstr00022786
WBCnstr00022790
WBCnstr00025849
Construct_productWBCnstr00018467
WBCnstr00018492
WBCnstr00018493
WBCnstr00021808
WBCnstr00025849
Regulate_expr_clusterWBPaper00049336:aptf-1(gk794)_downregulated_3-fold-embryo
WBPaper00049336:aptf-1(gk794)_downregulated_L4
WBPaper00049336:aptf-1(gk794)_upregulated_3-fold-embryo
WBPaper00049336:aptf-1(gk794)_upregulated_L4
Microarray_results (19)
Expression_cluster (94)
Interaction (50)
Map_infoMapIIPosition-0.231866Error0.002525
PositivePositive_cloneK06A1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (21)
RemarkMap 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