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WormBase Tree Display for Gene: WBGene00012936

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Name Class

WBGene00012936SMapS_parentSequenceY47D3A
IdentityVersion2
NameCGC_namepola-1Person_evidenceWBPerson30546
Sequence_nameY47D3A.29
Molecular_nameY47D3A.29
Y47D3A.29.1
CE32262
Other_nameCELE_Y47D3A.29Accession_evidenceNDBBX284603
Public_namepola-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:54WBPerson1971EventImportedInitial conversion from CDS class of WS125
205 Apr 2017 11:17:23WBPerson2970Name_changeCGC_namepola-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpola
Allele (164)
StrainWBStrain00051196
RNASeq_FPKM (74)
GO_annotation (27)
Contained_in_operonCEOP3720
Ortholog (42)
ParalogWBGene00008645Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021344Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionY47D3A.29 encodes the catalytic subunit of DNA polymerase alpha; large-scale RNAi screens indicate that Y47D3A.29 activity is essential for embryogenesis and required specifically for normal pronuclear migration, as well as normal nuclear position and cell division timing in early blastomeres.Paper_evidenceWBPaper00005654
WBPaper00006395
WBPaper00025054
Curator_confirmedWBPerson1843
Date_last_updated06 Apr 2007 00:00:00
Automated_descriptionPredicted to enable DNA binding activity; DNA-directed DNA polymerase activity; and chromatin binding activity. Predicted to be involved in lagging strand elongation; leading strand elongation; and mitotic DNA replication initiation. Predicted to be located in nucleus. Predicted to be part of alpha DNA polymerase:primase complex. Human ortholog(s) of this gene implicated in Van Esch-O'Driscoll syndrome and X-linked reticulate pigmentary disorder. Is an ortholog of human POLA1 (DNA polymerase alpha 1, catalytic 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_modelDOID:0111840Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9173)
DOID:0111834Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9173)
Molecular_infoCorresponding_CDSY47D3A.29
Corresponding_CDS_historyY47D3A.29:wp89
Y47D3A.29b:wp279
Corresponding_transcriptY47D3A.29.1
Other_sequence (28)
Associated_featureWBsf645602
WBsf645603
WBsf659569
WBsf659570
WBsf1015933
WBsf1015934
WBsf225798
Experimental_infoRNAi_resultWBRNAi00075442Inferred_automaticallyRNAi_primary
WBRNAi00026719Inferred_automaticallyRNAi_primary
WBRNAi00009341Inferred_automaticallyRNAi_primary
WBRNAi00056755Inferred_automaticallyRNAi_primary
WBRNAi00026720Inferred_automaticallyRNAi_primary
WBRNAi00097143Inferred_automaticallyRNAi_primary
WBRNAi00114561Inferred_automaticallyRNAi_primary
WBRNAi00009342Inferred_automaticallyRNAi_primary
Expr_patternExpr1012413
Expr1035733
Expr1160213
Expr2014989
Expr2033224
Microarray_results (23)
Expression_cluster (139)
Interaction (123)
Map_infoMapIIIPosition6.49087
PositivePositive_cloneY47D3AInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00031307
WBPaper00035228
WBPaper00038491
WBPaper00054520
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