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WormBase Tree Display for Gene: WBGene00012650

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Name Class

WBGene00012650SMapS_parentSequenceY39A1A
IdentityVersion2
NameCGC_nameorc-1Person_evidenceWBPerson195
Sequence_nameY39A1A.12
Molecular_nameY39A1A.12
Y39A1A.12.1
CE19131
Other_nameCELE_Y39A1A.12Accession_evidenceNDBBX284603
Public_nameorc-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:54WBPerson1971EventImportedInitial conversion from CDS class of WS125
217 Jun 2011 16:06:01WBPerson2970Name_changeCGC_nameorc-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classorc
Allele (45)
StrainWBStrain00005745
RNASeq_FPKM (74)
GO_annotation00104077
00104078
00104079
00104080
00104081
00104082
00104083
00104084
00119687
00119688
Contained_in_operonCEOP3692
Ortholog (38)
ParalogWBGene00000382Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionY39A1A.12 encodes a homolog of origin recognition complex 1, which is also a distant paralog of CDC-6; both Y39A1A.12 and CDC-6 encode homologs of the origin complex which, in yeast, controls the start of DNA replication; whether either Y39A1A.12 or CDC-6 are required for this function in C. elegans, individually or in parallel, is unknown.Paper_evidenceWBPaper00013079
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable ATP binding activity; ATP hydrolysis activity; and DNA binding activity. Predicted to be involved in DNA replication initiation and mitotic DNA replication checkpoint signaling. Predicted to be located in nucleus. Human ortholog(s) of this gene implicated in Meier-Gorlin syndrome 1. Is an ortholog of human ORC1 (origin recognition complex subunit 1).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:0080512Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8487)
Molecular_infoCorresponding_CDSY39A1A.12
Corresponding_transcriptY39A1A.12.1
Other_sequenceCRC09666_1
FC820332.1
Oden_isotig19249
CR01962
SRC07765_1
CBC05834_1
CJC00699_1
Hbac_isotig01464
CBC09470_1
CRC05891_1
Associated_featureWBsf645573
WBsf658535
WBsf225742
WBsf225743
WBsf225744
Experimental_infoRNAi_result (19)
Expr_patternExpr13394
Expr1019153
Expr1035590
Expr1159616
Expr2014633
Expr2032866
Construct_productWBCnstr00009673
Microarray_results (20)
Expression_cluster (169)
Interaction (154)
Map_infoMapIIIPosition4.21982Error0.030533
PositivePositive_cloneY39A1AInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00028564
WBPaper00038491
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