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WormBase Tree Display for Gene: WBGene00006367

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Name Class

WBGene00006367SMapS_parentSequenceCHROMOSOME_II
IdentityVersion2
NameCGC_namesym-2Person_evidenceWBPerson252
Sequence_nameZK1067.6
Molecular_nameZK1067.6a
ZK1067.6a.1
CE35148
ZK1067.6b
CE03707
ZK1067.6b.1
Other_nameCELE_ZK1067.6Accession_evidenceNDBBX284602
Public_namesym-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:40WBPerson1971EventImportedInitial conversion from geneace
219 Aug 2005 11:42:03WBPerson2970EventAcquires_mergeWBGene00014211
Acquires_mergeWBGene00014211
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsym
Allele (153)
Legacy_information[Herman RK] sym-2(mn617) by itself is essentially wild type but is synthetic lethal with any mec-8 loss-of-function mutation
StrainWBStrain00034404
RNASeq_FPKM (74)
GO_annotation (20)
Ortholog (49)
ParalogWBGene00013703Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00022253Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00020936Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionsym-2 encodes a predicted RNA binding protein that contains three RNA recognition motifs (RRMs) similar to those of Drosophila Fusilli and mammalian hnRNP F and H; genetic analyses indicate that, during embryonic development, sym-2 functions redundantly with mec-8, which also encodes an RRM-containing protein, to affect the structure of body wall muscles or their attachment to the body cuticle, perhaps by regulating maturation of transcripts essential for muscle development.Paper_evidenceWBPaper00003663
WBPaper00024639
Curator_confirmedWBPerson48
WBPerson1843
Date_last_updated04 May 2006 00:00:00
Automated_descriptionPredicted to enable mRNA binding activity. Involved in embryo development; embryonic body morphogenesis; and multicellular organismal movement. Predicted to be located in nucleoplasm. Predicted to be part of ribonucleoprotein complex. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 109. Is an ortholog of human ESRP1 (epithelial splicing regulatory protein 1) and ESRP2 (epithelial splicing regulatory protein 2).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:0111639Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:25966)
Molecular_infoCorresponding_CDSZK1067.6a
ZK1067.6b
Corresponding_CDS_historyZK1067.6:wp106
Corresponding_transcriptZK1067.6a.1
ZK1067.6b.1
Associated_feature (20)
Experimental_infoRNAi_resultWBRNAi00062554Inferred_automaticallyRNAi_primary
WBRNAi00095006Inferred_automaticallyRNAi_primary
WBRNAi00062552Inferred_automaticallyRNAi_primary
WBRNAi00022509Inferred_automaticallyRNAi_primary
WBRNAi00038138Inferred_automaticallyRNAi_primary
WBRNAi00062553Inferred_automaticallyRNAi_primary
WBRNAi00059094Inferred_automaticallyRNAi_primary
Expr_patternExpr1019298
Expr1032566
Expr1162524
Expr2017180
Expr2035316
Drives_constructWBCnstr00034387
Construct_productWBCnstr00034387
Microarray_results (19)
Expression_cluster (205)
Interaction (30)
Map_infoMapIIPosition1.09265Error0.000921
PositivePositive_cloneZK1067Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point7090
7091
Reference (18)
MethodGene