Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00021752

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00021752SMapS_parentSequenceY50D7A
IdentityVersion3
NameCGC_namexpd-1Paper_evidenceWBPaper00037879
Sequence_nameY50D7A.2
Molecular_nameY50D7A.2
Y50D7A.2.1
CE52547
Other_nameY50D7A.dCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
Y50D7A.h
CELE_Y50D7A.2Accession_evidenceNDBBX284603
Public_namexpd-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:04WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
221 Jul 2014 15:41:21WBPerson2970Name_changeCGC_namexpd-1
324 Nov 2017 12:02:54WBPerson1983EventAcquires_mergeWBGene00021759
Acquires_mergeWBGene00021759
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classxpd
Allele (375)
StrainWBStrain00055485
RNASeq_FPKM (74)
GO_annotation (25)
Contained_in_operonCEOP3851
CEOP3020
Ortholog (39)
ParalogWBGene00001049Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00009124Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010839Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00044493Caenorhabditis elegansFrom_analysisPanther
Structured_descriptionAutomated_descriptionPredicted to enable DNA helicase activity and damaged DNA binding activity. Predicted to be involved in positive regulation of mitotic recombination and transcription by RNA polymerase II. Predicted to be located in nucleus. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; gastrointestinal system cancer (multiple); hematologic cancer (multiple); and reproductive organ cancer (multiple). Is an ortholog of human ERCC2 (ERCC excision repair 2, TFIIH core complex helicase subunit).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_model (31)
Disease_relevanceMutations in human ERCC2 (orthologous to elegans Y50D7A.2 and yeast RAD3 genes) are associated with Cerebrooculofacioskeletal syndrome, Trichothiodystrophy and Xeroderma pigmentosum; ERCC2 is involved in DNA excision repair, with putative 5''-3'' DNA helicase activity, and may play a role in aging.Homo sapiensAccession_evidenceOMIM610756
601675
278730
126340
Curator_confirmedWBPerson324
Date_last_updated30 May 2012 00:00:00
Molecular_infoCorresponding_CDSY50D7A.2
Corresponding_CDS_historyY50D7A.2:wp99
Y50D7A.2:wp262
Y50D7A.2:wp263
Corresponding_transcriptY50D7A.2.1
Other_sequence (38)
Associated_featureWBsf991019
WBsf991020
WBsf991021
WBsf991022
WBsf1014036
WBsf1014037
WBsf1014038
WBsf1014039
WBsf224355
Experimental_infoRNAi_result (13)
Expr_patternExpr1011824
Expr1023886
Expr1039535
Expr1039542
Expr1160532
Expr1160535
Expr2007753
Expr2018103
Expr2025996
Expr2036241
Microarray_results (29)
Expression_cluster (95)
Interaction (166)
Map_infoPositivePositive_cloneY50D7AInferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionIII-26.9046
ReferenceWBPaper00027223
WBPaper00029038
WBPaper00031224
WBPaper00032410
WBPaper00038491
WBPaper00055090
WBPaper00062203
MethodGene