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WormBase Tree Display for Gene: WBGene00019481

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Name Class

WBGene00019481SMapS_parentSequenceK07C11
IdentityVersion2
NameCGC_namecogc-6Paper_evidenceWBPaper00026979
Person_evidenceWBPerson449
Sequence_nameK07C11.9
Molecular_nameK07C11.9
K07C11.9.1
CE07351
Other_nameCELE_K07C11.9Accession_evidenceNDBBX284605
Public_namecogc-6
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:01WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
216 Jan 2006 17:10:26WBPerson2970Name_changeCGC_namecogc-6
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcogc
Allele (33)
In_clusterconserved_miRNA_siRNA_cluster
RNASeq_FPKM (74)
GO_annotation00071029
00071030
00071031
00071032
00071033
00071034
00071035
00071036
00124323
00124324
Ortholog (39)
Structured_descriptionConcise_descriptioncogc-6 encodes an ortholog of mammalian COG-6, a subunit of lobe B ofthe conserved oligomeric Golgi complex (COGC); COGC-6 is weakly requiredfor normal gonadal distal tip cell migration, a process that alsorequires seven other orthologs of COGC subunits; like other lobe Bsubunits in both C. elegans and S. cerevisiae, COGC-6 is only partiallyrequired for normal function, while lobe A subunits are stronglyrequired in either worms or yeast.Paper_evidenceWBPaper00026979
WBPaper00028363
WBPaper00028599
WBPaper00028603
Curator_confirmedWBPerson567
Date_last_updated25 Oct 2006 00:00:00
Automated_descriptionInvolved in gonad morphogenesis and regulation of cell migration. Predicted to be located in Golgi membrane. Predicted to be part of Golgi transport complex. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIl. Is an ortholog of human COG6 (component of oligomeric golgi complex 6).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:0070264Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18621)
Molecular_infoCorresponding_CDSK07C11.9
Corresponding_transcriptK07C11.9.1
Other_sequenceCR01125
CBC01817_1
CR09438
CRC04217_1
CBC00410_1
FD515230.1
CSC01446_1
Associated_featureWBsf652832
WBsf668666
WBsf669150
WBsf1000599
WBsf1019992
WBsf234047
WBsf234048
WBsf234049
Experimental_infoRNAi_resultWBRNAi00016704Inferred_automaticallyRNAi_primary
WBRNAi00064304Inferred_automaticallyRNAi_primary
WBRNAi00076551Inferred_automaticallyRNAi_primary
WBRNAi00095102Inferred_automaticallyRNAi_primary
WBRNAi00099108Inferred_automaticallyRNAi_primary
WBRNAi00095103Inferred_automaticallyRNAi_primary
WBRNAi00050127Inferred_automaticallyRNAi_primary
WBRNAi00034056Inferred_automaticallyRNAi_primary
WBRNAi00002384Inferred_automaticallyRNAi_primary
Expr_patternExpr1027185
Expr1038417
Expr1153828
Expr2010295
Expr2028537
Drives_constructWBCnstr00025808
Construct_productWBCnstr00025808
Microarray_results (21)
Expression_cluster (96)
Interaction (37)
Map_infoMapVPosition1.22329Error0.010338
PositivePositive_cloneK07C11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5659
4928
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00041771
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