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WormBase Tree Display for Gene: WBGene00001089

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Name Class

WBGene00001089SMapS_parentSequenceCHROMOSOME_V
IdentityVersion3
NameCGC_namedre-1Person_evidenceWBPerson759
Sequence_nameK04A8.6
Molecular_nameK04A8.6a
K04A8.6a.1
CE27388
K04A8.6b
CE50130
K04A8.6a.2
K04A8.6b.1
Other_nameF46E10.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
fbxo-11.1Person_evidenceWBPerson171
CELE_K04A8.6Accession_evidenceNDBBX284605
Public_namedre-1
DB_infoDatabaseAceViewgene5H14
WormQTLgeneWBGene00001089
WormFluxgeneWBGene00001089
NDBlocus_tagCELE_K04A8.6
PanthergeneCAEEL|WormBase=WBGene00001089|UniProtKB=Q94251
familyPTHR22990
NCBIgene179045
RefSeqproteinNM_001392535.1
NM_001380672.1
SwissProtUniProtAccQ94251
TrEMBLUniProtAccA0A0K3AS68
UniProt_GCRPUniProtAccQ94251
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
214 Mar 2007 09:19:48WBPerson2970EventAcquires_mergeWBGene00019377
Name_changeSequence_nameK04A8.6
312 Jan 2023 20:48:33WBPerson51134Name_changeCGC_namedre-1
Other_namefbxo-11.1
Acquires_mergeWBGene00019377
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdre
Allele (179)
StrainWBStrain00001341
WBStrain00002251
WBStrain00036922
WBStrain00037225
WBStrain00000025
RNASeq_FPKM (74)
GO_annotation (27)
Ortholog (42)
ParalogWBGene00015268Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptiondre-1 encodes an ortholog of human FBXO11/PRMT9 (OMIM:607871, associatedwith vitiligo and otitis media) that is required, in conjunction withDAF-12 and its partners, for global developmental timing of thetransistion from larval to adult cell fates; DRE-1 has an N-terminalF-box domain, three central tandem C-terminal CASH domains, and aC-terminal zinc finger; hypomorphic dre-1 mutations are syntheticallyheterochronic with loss-of-function daf-12 alleles, inducing defectivedistal tip cell migration and precocious fusion of seam cells; fivedifferent hypomorphic dre-1 alleles alter conserved glycine residues inthe CASH domain region, whereas the null dre-1(hd60) allele is lethal atthe three-fold embryo stage; DRE-1 is expressed in many tissues,including epidermal and distal tip cells, and localizes to both nucleusand cytoplasm; strong loss-of-function of dre-1 (the dh99 mutant fedRNAi) induces defects at all four molts; dre-1 also has syntheticphenotypes with daf-9(k182), daf-36(k114), and lin-29(n546); dre-1-likeenhancement of daf-12 is also seen in skr-1(RNAi), cul-1(RNAi), orrbx-1/2(RNAi) animals; DRE-1 and SKR-1 bind one another, as do theirhuman orthologs; DRE-1 affects lin-29 expression, and is suppressed bylin-42(RNAi); DRE-1 is paralogous to C. elegans BE0003N10.3.Paper_evidenceWBPaper00012854
WBPaper00029151
WBPaper00029159
WBPaper00029160
WBPaper00029161
WBPaper00029162
Curator_confirmedWBPerson567
Date_last_updated12 Mar 2007 00:00:00
Automated_descriptionPredicted to enable zinc ion binding activity. Involved in several processes, including mesodermal cell migration; nematode larval development; and positive regulation of apoptotic process involved in development. Located in cytoplasm and nucleus. Expressed in several structures, including P5.ppp; gonad; hypodermis; non-striated muscle; and vulva. Human ortholog(s) of this gene implicated in breast carcinoma; gastrointestinal system cancer (multiple); and lung non-small cell carcinoma. Is an ortholog of human FBXO11 (F-box protein 11).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:3908Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13590)
DOID:3459Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13590)
DOID:10534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13590)
DOID:684Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13590)
Molecular_infoCorresponding_CDSK04A8.6a
K04A8.6b
Corresponding_transcriptK04A8.6a.1
K04A8.6a.2
K04A8.6b.1
Other_sequence (34)
Associated_feature (17)
Experimental_infoRNAi_result (19)
Expr_pattern (13)
Drives_constructWBCnstr00000395
WBCnstr00000396
WBCnstr00000397
WBCnstr00000401
WBCnstr00002234
WBCnstr00004264
WBCnstr00017520
WBCnstr00019163
WBCnstr00037087
Construct_productWBCnstr00000395
WBCnstr00000396
WBCnstr00000397
WBCnstr00000401
WBCnstr00019163
WBCnstr00037087
Microarray_results (21)
Expression_cluster (172)
InteractionWBInteraction000032451
WBInteraction000052706
WBInteraction000052707
WBInteraction000322896
WBInteraction000326800
WBInteraction000327371
WBInteraction000337887
WBInteraction000346773
WBInteraction000357436
WBInteraction000381413
WBInteraction000385263
WBInteraction000411036
WBInteraction000413558
WBInteraction000426530
WBInteraction000438847
WBInteraction000500896
WBInteraction000500897
WBInteraction000500898
WBInteraction000500901
WBInteraction000500902
WBInteraction000502832
WBInteraction000503207
WBInteraction000519311
WBInteraction000521439
WBInteraction000521440
WBInteraction000521441
WBInteraction000523636
WBInteraction000523637
WBInteraction000540050
WBInteraction000540908
WBInteraction000548104
WBInteraction000556344
WBInteraction000560764
WBInteraction000560765
WBInteraction000568260
WBInteraction000573406
WBInteraction000583591
WBInteraction000583592
Map_infoMapVPosition0.05417Error0.006328
PositivePositive_cloneK04A8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (26)
Remarkdre-1 was found in an EMS screen for daf-12 redundant functions [Fielenbach N][030331 ck1]
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