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WormBase Tree Display for Gene: WBGene00015692

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Name Class

WBGene00015692SMapS_parentSequenceC10H11
IdentityVersion2
NameCGC_nameugt-25Person_evidenceWBPerson1208
WBPerson655
Sequence_nameC10H11.3
Molecular_nameC10H11.3
C10H11.3.1
CE08092
Other_nameCELE_C10H11.3Accession_evidenceNDBBX284601
Public_nameugt-25
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:56WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
210 Jun 2005 11:17:00WBPerson2970Name_changeCGC_nameugt-25
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classugt
AlleleWBVar01911578
WBVar02127223
WBVar00153326
WBVar00153327
WBVar00153328
WBVar00633899
WBVar00633900
WBVar00633901
WBVar00633902
WBVar00633903
WBVar00633904
WBVar00633905
WBVar00633906
WBVar00633907
WBVar00633908
WBVar00633909
WBVar01499919
WBVar01475446
WBVar00633910
WBVar00633911
WBVar00633912
WBVar00633913
WBVar00633914
WBVar00633915
WBVar00633916
WBVar00633917
WBVar00633918
WBVar00633919
WBVar00633920
WBVar00633921
WBVar00633922
WBVar00275820
WBVar00333062
WBVar00333063
WBVar00333064
WBVar00333065
WBVar01499786
WBVar00297975
WBVar01499985
WBVar01282522
WBVar01956986
WBVar00091031
WBVar01573975
WBVar01498959
WBVar01911577
RNASeq_FPKM (74)
GO_annotation00049839
00049840
00049841
00049842
00049843
00049844
00049845
00049846
00121493
Ortholog (102)
Paralog (75)
Structured_descriptionAutomated_descriptionPredicted to enable UDP-glycosyltransferase activity. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in osteoporosis. Is an ortholog of several human genes including UGT2B15 (UDP glucuronosyltransferase family 2 member B15); UGT2B4 (UDP glucuronosyltransferase family 2 member B4); and UGT2B7 (UDP glucuronosyltransferase family 2 member B7).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:11476Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12547)
Molecular_infoCorresponding_CDSC10H11.3
Corresponding_transcriptC10H11.3.1
Other_sequenceCJC03647_1
CJC05355_1
AS10156
EX559766.1
ACC12378_1
ASC04370_1
Associated_featureWBsf643234
WBsf643235
WBsf656244
WBsf217573
Experimental_infoRNAi_resultWBRNAi00040333Inferred_automaticallyRNAi_primary
WBRNAi00028799Inferred_automaticallyRNAi_primary
WBRNAi00002939Inferred_automaticallyRNAi_primary
Expr_patternExpr1023135
Expr1036717
Expr1144402
Expr2017770
Expr2035908
Drives_constructWBCnstr00028647
Construct_productWBCnstr00028647
Microarray_results (19)
Expression_cluster (245)
InteractionWBInteraction000504188
Map_infoMapIPosition-0.77257Error0.008513
PositivePositive_cloneC10H11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00044018
WBPaper00055090
WBPaper00055433
WBPaper00062388
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