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WormBase Tree Display for Gene: WBGene00001439

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Name Class

WBGene00001439EvidencePerson_evidenceWBPerson266
WBPerson411
SMapS_parentSequenceF26D12
IdentityVersion1
NameCGC_namefkh-7Person_evidenceWBPerson411
Sequence_nameF26D12.1
Molecular_name (44)
Other_nameF26D12.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
F26D12.bCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_F26D12.1Accession_evidenceNDBBX284604
Public_namefkh-7
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfkh
Allele (277)
StrainWBStrain00036765
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (27)
Structured_descriptionConcise_descriptionfkh-7 encodes one of 15 forkhead transcriptional regulators encoded by the C. elegans genome; by homology, FKH-7 is predicted to function as a transcription factor that regulates gene expression during development; however, as loss of fkh-7 activity via RNA-mediated interference (RNAi) does not result in any obvious abnormalities, the precise role of FKH-7 in C. elegans development and/or behavior is not yet known; however, reporter gene studies indicate that fkh-7 expression is detected only in neurons of the head and tail ganglia, the nerve cord, and the male tail, suggesting that FKH-7 likely functions in nervous system differentiation.Paper_evidenceWBPaper00005730
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Expressed in several structures, including intestine; neurons; pharynx; reproductive system; and ventral nerve cord. Human ortholog(s) of this gene implicated in several diseases, including carcinoma (multiple); communication disorder (multiple); and tuberculosis (multiple). Is an ortholog of human FOXP2 (forkhead box P2).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_model (41)
Molecular_infoCorresponding_CDS (14)
Corresponding_CDS_historyF26D12.1:wp83
F26D12.1:wp96
F26D12.1a:wp115
F26D12.1b:wp115
F26D12.1c:wp115
F26D12.1c:wp240
F26D12.1d:wp122
F26D12.1d:wp240
Corresponding_transcript (16)
Other_sequence (22)
Associated_feature (26)
Transcription_factorWBTranscriptionFactor000170
Experimental_infoRNAi_result (13)
Expr_pattern (13)
Drives_constructWBCnstr00010774
WBCnstr00010775
WBCnstr00014252
WBCnstr00014253
WBCnstr00014292
WBCnstr00014293
WBCnstr00014342
WBCnstr00014351
WBCnstr00036947
Construct_productWBCnstr00036947
WBCnstr00038842
Microarray_results (43)
Expression_cluster (183)
Interaction (15)
Map_infoMapIVPosition1.89836Error0.001556
PositivePositive_cloneF26D12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (11)
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