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WormBase Tree Display for Gene: WBGene00010230

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Name Class

WBGene00010230SMapS_parentSequenceF58A4
IdentityVersion2
NameCGC_namerpac-19Person_evidenceWBPerson10054
Sequence_nameF58A4.9
Molecular_nameF58A4.9
F58A4.9.1
CE00225
Other_nameCELE_F58A4.9Accession_evidenceNDBBX284603
Public_namerpac-19
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
228 Sep 2012 14:29:00WBPerson2970Name_changeCGC_namerpac-19
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrpac
AlleleWBVar00092985Inferred_automaticallyFrom strain object: VC1325
WBVar00851575
WBVar01645909
WBVar01500260
WBVar00405717
WBVar01499774
WBVar01723199
WBVar01332159
WBVar00851574
StrainWBStrain00036516
RNASeq_FPKM (74)
GO_annotation00044463
00044464
00044465
00044466
00044467
00044468
00044469
00044470
00121655
00121656
Contained_in_operonCEOP3608
Ortholog (31)
ParalogWBGene00012187Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable protein dimerization activity. Predicted to contribute to RNA polymerase I activity. Predicted to be involved in transcription by RNA polymerase III and transcription elongation by RNA polymerase I. Predicted to be located in nucleus. Predicted to be part of RNA polymerase I complex and RNA polymerase III complex. Used to study obesity. Human ortholog(s) of this gene implicated in Treacher Collins syndrome 2. Is an ortholog of human POLR1D (RNA polymerase I and III subunit D).Paper_evidenceWBPaper00065943
WBPaper00067038
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS296 version of WormBase
Date_last_updated20 Mar 2025 00:00:00
Disease_infoExperimental_modelDOID:9970Homo sapiensPaper_evidenceWBPaper00061889
Curator_confirmedWBPerson324
Date_last_updated28 Jun 2022 00:00:00
Potential_modelDOID:0080790Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20422)
Models_disease_in_annotationWBDOannot00001261
Molecular_infoCorresponding_CDSF58A4.9
Corresponding_transcriptF58A4.9.1
Other_sequence (27)
Associated_featureWBsf651391
WBsf993736
Experimental_infoRNAi_result (26)
Expr_patternExpr1014907
Expr1034461
Expr1152674
Expr2015417
Expr2033652
Drives_constructWBCnstr00031569
Construct_productWBCnstr00031569
Microarray_results (19)
Expression_cluster (143)
Interaction (186)
Map_infoMapIIIPosition0.819375
PositivePositive_cloneF58A4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00049828
WBPaper00055090
WBPaper00061889
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