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WormBase Tree Display for Gene: WBGene00003154

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Name Class

WBGene00003154EvidenceCGC_data_submission
SMapS_parentSequenceY17G7B
IdentityVersion1
NameCGC_namemcm-2Person_evidenceWBPerson1160
Sequence_nameY17G7B.5
Molecular_nameY17G7B.5a
Y17G7B.5a.1
CE19038
Other_nameCELE_Y17G7B.5Accession_evidenceNDBBX284602
Public_namemcm-2
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmcm
Allele (132)
StrainWBStrain00001383
RNASeq_FPKM (74)
GO_annotation (32)
Ortholog (39)
ParalogWBGene00003158Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003156Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003157Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003155Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003159Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable single-stranded DNA binding activity. Predicted to contribute to 3'-5' DNA helicase activity and single-stranded DNA helicase activity. Predicted to be involved in DNA unwinding involved in DNA replication; double-strand break repair via break-induced replication; and mitotic DNA replication initiation. Located in condensed chromosome and pronucleus. Expressed in excretory cell; intestine; and uterus. Human ortholog(s) of this gene implicated in Alzheimer's disease and autosomal dominant nonsyndromic deafness 70. Is an ortholog of human MCM2 (minichromosome maintenance complex component 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:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6944)
DOID:0110592Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6944)
Molecular_infoCorresponding_CDSY17G7B.5a
Corresponding_CDS_historyY17G7B.5b:wp282
Corresponding_transcriptY17G7B.5a.1
Other_sequence (75)
Associated_featureWBsf650639
WBsf989989
WBsf1013372
WBsf224023
Experimental_infoRNAi_result (14)
Expr_pattern (11)
Drives_constructWBCnstr00002274
WBCnstr00004282
Construct_productWBCnstr00009676
WBCnstr00042162
AntibodyWBAntibody00002757
Microarray_results (28)
Expression_cluster (218)
Interaction (224)
Map_infoMapIIPosition5.67515Error0.063403
PositivePositive_cloneY17G7BInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (14)
RemarkSequence connection from [Kim SK]
Map 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