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WormBase Tree Display for Gene: WBGene00009939

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Name Class

WBGene00009939SMapS_parentSequenceF52F12
IdentityVersion4
NameCGC_nameztf-11Person_evidenceWBPerson524
WBPerson1997
Sequence_nameF52F12.6
Molecular_nameF52F12.6a
F52F12.6a.1
CE24995
F52F12.6b
CE46793
F52F12.6b.1
Other_nameekl-2Paper_evidenceWBPaper00031487
CELE_F52F12.6Accession_evidenceNDBBX284601
Public_nameztf-11
DB_infoDatabaseAceViewgene1K482
WormQTLgeneWBGene00009939
WormFluxgeneWBGene00009939
NDBlocus_tagCELE_F52F12.6
NCBIgene172845
RefSeqproteinNM_001264316.3
NM_001264317.3
SwissProtUniProtAccO02274
TREEFAMTREEFAM_IDTF317299
UniProt_GCRPUniProtAccO02274
OMIMgene613084
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
218 Jul 2005 13:34:00WBPerson2970Name_changeCGC_nameekl-2
322 Oct 2007 15:16:41WBPerson2970Name_changeCGC_nameztf-11
420 Feb 2008 16:59:39WBPerson2970Name_changeOther_nameztf-11
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classztf
Allele (70)
StrainWBStrain00031537
WBStrain00030095
WBStrain00030097
RNASeq_FPKM (74)
GO_annotation (17)
Ortholog (40)
ParalogWBGene00010867Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable zinc ion binding activity. Involved in several processes, including negative regulation of transcription by RNA polymerase II; neuron differentiation; and positive regulation of cell differentiation. Located in nucleus. Expressed in g1 and head neurons. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder 39. Is an ortholog of human MYT1L (myelin transcription factor 1 like).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:0070069Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7623)
Molecular_infoCorresponding_CDSF52F12.6a
F52F12.6b
Corresponding_transcriptF52F12.6a.1
F52F12.6b.1
Other_sequenceJI169553.1
Dviv_isotig18198
Dviv_isotig18199
Associated_feature (17)
Gene_product_binds (297)
Transcription_factorWBTranscriptionFactor000759
Experimental_infoRNAi_resultWBRNAi00082504Inferred_automaticallyRNAi_primary
WBRNAi00003743Inferred_automaticallyRNAi_primary
WBRNAi00116763Inferred_automaticallyRNAi_primary
WBRNAi00000286Inferred_automaticallyRNAi_primary
WBRNAi00048012Inferred_automaticallyRNAi_primary
WBRNAi00070207Inferred_automaticallyRNAi_primary
WBRNAi00082618Inferred_automaticallyRNAi_primary
Expr_patternExpr427
Expr1020528
Expr1034330
Expr1151827
Expr1200080
Expr1200081
Expr2018185
Expr2036322
Drives_constructWBCnstr00037854
Construct_productWBCnstr00016725
WBCnstr00018914
WBCnstr00037854
Regulate_expr_clusterWBPaper00057143:ztf-11(RNAi)_downregulated
WBPaper00057143:ztf-11(RNAi)_upregulated
Microarray_results (20)
Expression_cluster (221)
Interaction (40)
Map_infoMapIPosition4.05133Error0.011125
PositivePositive_cloneF52F12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5407
5060
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00040002
WBPaper00055090
WBPaper00057143
WBPaper00057179
WBPaper00061738
WBPaper00062585
WBPaper00064339
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