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WormBase Tree Display for Gene: WBGene00003904

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Name Class

WBGene00003904EvidenceAuthor_evidenceSlack FJ
SMapS_parentSequenceC17E4
IdentityVersion2
NameCGC_namepabp-2Person_evidenceWBPerson2384
WBPerson599
Sequence_nameC17E4.5
Molecular_nameC17E4.5
C17E4.5.1
CE08254
Other_namepab-3Person_evidenceWBPerson1160
CELE_C17E4.5Accession_evidenceNDBBX284601
Public_namepabp-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
223 Feb 2007 15:37:00WBPerson2970Name_changeCGC_namepabp-2
Other_namepab-3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpabp
Allele (19)
StrainWBStrain00001368
WBStrain00036043
RNASeq_FPKM (74)
GO_annotation00085568
00085569
00085570
00085571
00111974
00111975
Contained_in_operonCEOP1543
CEOP192
Ortholog (48)
Structured_descriptionConcise_descriptionpabp-2 encodes the C. elegans PABPN1 (polyadenylate-binding protein, nuclear 1) ortholog; by homology, PABP-2 is predicted to function as a poly(A)-binding protein involved in several aspects of pre-mRNA processing; large-scale RNAi screens indicate that pabp-2 activity is essential for embryonic and larval development, as well as normal rates of growth and locomotion; in humans, expansion of a polyalanine repeat in PABPN1 is associated with oculopharyngeal muscular dystrophy (OPMD, OMIM:602279).Paper_evidenceWBPaper00004402
WBPaper00005599
WBPaper00006395
WBPaper00024497
WBPaper00025054
WBPaper00031237
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated27 Nov 2007 00:00:00
Automated_descriptionPredicted to enable poly(A) binding activity. Predicted to be located in nucleus. Human ortholog(s) of this gene implicated in oculopharyngeal muscular dystrophy. Is an ortholog of human PABPN1 (poly(A) binding protein nuclear 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:11719Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8565)
Molecular_infoCorresponding_CDSC17E4.5
Corresponding_transcriptC17E4.5.1
Other_sequence (45)
Associated_featureWBsf976898
WBsf220082
WBsf220083
WBsf220084
Experimental_infoRNAi_result (20)
Expr_patternChronogram862
Expr5285
Expr1026265
Expr1031841
Expr1144842
Expr2014676
Expr2032909
Drives_constructWBCnstr00002258
WBCnstr00035805
Construct_productWBCnstr00016328
WBCnstr00035805
AntibodyWBAntibody00002247
Microarray_results (20)
Expression_cluster (121)
Interaction (116)
Map_infoMapIPosition3.76033Error0.000569
PositivePositive_cloneC17E4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5225
Pseudo_map_position
ReferenceWBPaper00027281
WBPaper00031006
WBPaper00038240
WBPaper00038491
WBPaper00048493
WBPaper00055090
WBPaper00059527
WBPaper00064339
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