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WormBase Tree Display for Gene: WBGene00010716

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Name Class

WBGene00010716SMapS_parentSequenceK09C8
IdentityVersion2
NameCGC_namelge-1Person_evidenceWBPerson345
Sequence_nameK09C8.4
Molecular_nameK09C8.4
K09C8.4.1
CE44089
Other_nameCELE_K09C8.4Accession_evidenceNDBBX284606
Public_namelge-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
215 Nov 2004 13:50:18WBPerson2970Name_changeCGC_namelge-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlge
Allele (50)
RNASeq_FPKM (74)
GO_annotation00071496
00071497
00071498
00071499
00071500
00071501
00071502
00071503
00071504
00118069
Ortholog (47)
ParalogWBGene00008290Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00008491Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00010167Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00010694Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00017723Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00011779Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00015982Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00009032Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable glucuronosyltransferase activity and xylosyltransferase activity. Predicted to be involved in protein O-linked mannosylation. Predicted to be located in Golgi apparatus. Human ortholog(s) of this gene implicated in congenital muscular dystrophy-dystroglycanopathy type A6 and muscular dystrophy-dystroglycanopathy type B6. Is an ortholog of human LARGE2 (LARGE xylosyl- and glucuronyltransferase 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:0111242Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6511)
DOID:0110637Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6511)
Molecular_infoCorresponding_CDSK09C8.4
Corresponding_CDS_historyK09C8.4:wp122
K09C8.4:wp196
K09C8.4:wp206
Corresponding_transcriptK09C8.4.1
Other_sequenceJI474807.1
JI469136.1
Associated_featureWBsf1006870
WBsf236323
Experimental_infoRNAi_resultWBRNAi00016894Inferred_automaticallyRNAi_primary
WBRNAi00034198Inferred_automaticallyRNAi_primary
WBRNAi00092980Inferred_automaticallyRNAi_primary
WBRNAi00050403Inferred_automaticallyRNAi_primary
Expr_patternExpr1012020
Expr1154106
Expr2013141
Expr2031373
Drives_constructWBCnstr00031199
Construct_productWBCnstr00031199
Microarray_results (19)
Expression_cluster (107)
Map_infoMapXPosition2.77227Error0.007934
PositivePositive_cloneK09C8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4566
4899
Pseudo_map_position
ReferenceWBPaper00038491
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