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WormBase Tree Display for Gene: WBGene00017814

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Name Class

WBGene00017814SMapS_parentSequenceF26A10
IdentityVersion1
NameSequence_nameF26A10.2
Molecular_nameF26A10.2
F26A10.2.1
CE02692
F26A10.2.2
Other_nameCELE_F26A10.2Accession_evidenceNDBBX284606
Public_nameF26A10.2
DB_infoDatabaseAceViewgeneXI252
WormQTLgeneWBGene00017814
WormFluxgeneWBGene00017814
NDBlocus_tagCELE_F26A10.2
PanthergeneCAEEL|WormBase=WBGene00017814|UniProtKB=Q19807
familyPTHR24404
NCBIgene181025
RefSeqproteinNM_076889.5
TrEMBLUniProtAccQ19807
UniProt_GCRPUniProtAccQ19807
OMIMgene608433
613915
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (232)
RNASeq_FPKM (74)
GO_annotation00065921
00065922
00065923
00065924
Ortholog (44)
Paralog (15)
Structured_descriptionConcise_descriptionF26A10.2 encodes a protein with four zinc-finger domains and a glutamine/asparagine-rich domain, that is required for maintenance of the germline and for locomotion; F26A10.2(RNAi) animals are uncoordinated and have sterile progeny.Paper_evidenceWBPaper00005068
WBPaper00005654
WBPaper00012788
WBPaper00012830
WBPaper00012882
WBPaper00012897
WBPaper00013003
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable chromatin insulator sequence binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromosome. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder 22 and lethal congenital contracture syndrome. Is an ortholog of human ZBTB18 (zinc finger and BTB domain containing 18); ZBTB42 (zinc finger and BTB domain containing 42); and ZNF148 (zinc finger protein 148).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:0060558Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:32550)
DOID:0070052Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:13030)
Molecular_infoCorresponding_CDSF26A10.2
Corresponding_transcriptF26A10.2.1
F26A10.2.2
Other_sequenceJI166539.1
Oden_isotig24106
Associated_feature (22)
Transcription_factorWBTranscriptionFactor000995
Experimental_infoRNAi_resultWBRNAi00025237Inferred_automaticallyRNAi_primary
WBRNAi00031423Inferred_automaticallyRNAi_primary
WBRNAi00071622Inferred_automaticallyRNAi_primary
WBRNAi00008701Inferred_automaticallyRNAi_primary
WBRNAi00045586Inferred_automaticallyRNAi_primary
Expr_patternExpr1024003
Expr1037655
Expr1149497
Expr2002995
Expr2021211
Drives_constructWBCnstr00026995
Construct_productWBCnstr00026995
Microarray_results (20)
Expression_cluster (178)
Interaction (20)
Map_infoPositivePositive_cloneF26A10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionX-1.44354
ReferenceWBPaper00038491
MethodGene