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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)
Interaction (38)
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