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WormBase Tree Display for Gene: WBGene00009542

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Name Class

WBGene00009542SMapS_parentSequenceF38E11
IdentityVersion2
NameCGC_namecopb-2Person_evidenceWBPerson3188
Sequence_nameF38E11.5
Molecular_nameF38E11.5
F38E11.5.1
CE18673
Other_nameCELE_F38E11.5Accession_evidenceNDBBX284604
Public_namecopb-2
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
208 Aug 2013 16:41:57WBPerson2970Name_changeCGC_namecopb-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcopb
Allele (60)
StrainWBStrain00051353
RNASeq_FPKM (74)
GO_annotation (21)
Ortholog (40)
ParalogWBGene00008476Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00022119Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00270321Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionF38E11.5 encodes a beta' (beta-prime) subunit of the coatomer (COPI) complex; in mass RNAi assays, F38E11.5 is required for fertility and general health.Paper_evidenceWBPaper00005654
WBPaper00006395
WBPaper00012764
WBPaper00012858
WBPaper00012863
WBPaper00012889
WBPaper00013106
WBPaper00013627
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable structural molecule activity. Involved in embryo development; intracellular protein transport; and oocyte development. Predicted to be located in COPI-coated vesicle membrane and Golgi membrane. Predicted to be part of COPI vesicle coat. Human ortholog(s) of this gene implicated in primary autosomal recessive microcephaly 19. Is an ortholog of human COPB2 (COPI coat complex subunit beta 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:0070281Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2232)
Molecular_infoCorresponding_CDSF38E11.5
Corresponding_transcriptF38E11.5.1
Other_sequence (42)
Associated_featureWBsf646235
WBsf660509
WBsf997425
WBsf1017967
WBsf228831
WBsf228832
WBsf228833
WBsf228834
Experimental_infoRNAi_result (15)
Expr_patternExpr1024749
Expr1034170
Expr1150600
Expr2010457
Expr2028697
Drives_constructWBCnstr00032114
Construct_productWBCnstr00032114
Microarray_results (25)
Expression_cluster (119)
Interaction (107)
Map_infoMapIVPosition4.27042
PositivePositive_cloneF38E11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00003831
WBPaper00018551
WBPaper00027057
WBPaper00038491
WBPaper00049828
WBPaper00055090
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