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WormBase Tree Display for Gene: WBGene00007914

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Name Class

WBGene00007914SMapS_parentSequenceC34B7
IdentityVersion2
NameCGC_namemys-4Person_evidenceWBPerson2693
WBPerson552
WBPerson268
Sequence_nameC34B7.4
Molecular_nameC34B7.4
C34B7.4.1
CE27818
Other_nameCELE_C34B7.4Accession_evidenceNDBBX284601
Public_namemys-4
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
207 Apr 2008 14:21:37WBPerson2970Name_changeCGC_namemys-4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmys
Allele (36)
RNASeq_FPKM (74)
GO_annotation (12)
Contained_in_operonCEOP1464
Ortholog (35)
ParalogWBGene00007029Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00016200Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010537Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00045419Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00018013Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionC34B7.4 encodes a MYST family histone acetyltransferase; based upon sequence similarity, the product of C34B7.4 is predicted to be the enzymatic component of an NuA4-like histone acetyltransferase (HAT) complex that functions in transcriptional activation; C34B7.4 is likely required for regulating gene expression in multiple tissues, as loss of its activity via RNAi results in suppression of ectopic lag-2 reporter expression seen in intestinal tissue in SynMuv B mutants as well as in some suppression of the lin-15AB SynMuv phenotype.Paper_evidenceWBPaper00013412
WBPaper00027634
Curator_confirmedWBPerson1843
Date_last_updated11 Jun 2007 00:00:00
Automated_descriptionPredicted to enable histone H4K16 acetyltransferase activity and transcription coregulator activity. Predicted to be involved in negative regulation of DNA-templated transcription and positive regulation of transcription by RNA polymerase II. Predicted to be part of MSL complex. Human ortholog(s) of this gene implicated in androgen insensitivity syndrome and breast cancer. Is an ortholog of human KAT7 (lysine acetyltransferase 7).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:4674Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17016)
DOID:1612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17016)
Molecular_infoCorresponding_CDSC34B7.4
Corresponding_transcriptC34B7.4.1
Other_sequence (23)
Associated_featureWBsf643525
WBsf656626
WBsf656627
WBsf218145
WBsf218146
WBsf218147
Experimental_infoRNAi_result (11)
Expr_patternExpr1017710
Expr1033428
Expr1145856
Expr2013850
Expr2032090
Drives_constructWBCnstr00033385
Construct_productWBCnstr00033385
Microarray_results (19)
Expression_cluster (122)
InteractionWBInteraction000051554
WBInteraction000051590
WBInteraction000051619
WBInteraction000051661
WBInteraction000552465
WBInteraction000553666
WBInteraction000582754
Map_infoMapIPosition2.7464Error0.002289
PositivePositive_cloneC34B7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00013412
WBPaper00027634
WBPaper00036007
WBPaper00038372
WBPaper00038491
WBPaper00042680
WBPaper00055090
WBPaper00060474
WBPaper00065308
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