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WormBase Tree Display for Gene: WBGene00012714

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Name Class

WBGene00012714SMapS_parentSequenceY39E4B
IdentityVersion3
NameCGC_nameabce-1Paper_evidenceWBPaper00028961
Sequence_nameY39E4B.1
Molecular_nameY39E4B.1
Y39E4B.1.1
CE21713
Other_nametag-351Person_evidenceWBPerson201
CELE_Y39E4B.1Accession_evidenceNDBBX284603
Public_nameabce-1
DB_infoDatabaseAceViewgene3O249
WormQTLgeneWBGene00012714
WormFluxgeneWBGene00012714
NDBlocus_tagCELE_Y39E4B.1
PanthergeneCAEEL|WormBase=WBGene00012714|UniProtKB=Q9U2K8
familyPTHR19248
NCBIgene176733
RefSeqproteinNM_067316.8
TREEFAMTREEFAM_IDTF105206
TrEMBLUniProtAccQ9U2K8
UniProt_GCRPUniProtAccQ9U2K8
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:54WBPerson1971EventImportedInitial conversion from CDS class of WS125
221 Jun 2005 09:45:25WBPerson2970Name_changeCGC_nametag-351
321 Jun 2007 14:37:04WBPerson2970Name_changeCGC_nameabce-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classabce
Allele (86)
StrainWBStrain00001519
WBStrain00036276
RNASeq_FPKM (74)
GO_annotation00099349
00099350
00099351
00099352
00099353
00099354
00099355
00099356
00119744
00119745
Contained_in_operonCEOP3819
Ortholog (43)
Structured_descriptionAutomated_descriptionPredicted to enable ATP binding activity; iron ion binding activity; and ribosomal small subunit binding activity. Predicted to be involved in ribosomal subunit export from nucleus; translational initiation; and translational termination. Expressed in several structures, including muscle cell; neurons; and vulva. Human ortholog(s) of this gene implicated in breast carcinoma; carcinoma (multiple); and human immunodeficiency virus infectious disease. Is an ortholog of human ABCE1 (ATP binding cassette subfamily E member 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:3910Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:69)
DOID:3459Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:69)
DOID:526Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:69)
DOID:684Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:69)
Molecular_infoCorresponding_CDSY39E4B.1
Corresponding_transcriptY39E4B.1.1
Other_sequence (91)
Associated_featureWBsf659692
WBsf659693
WBsf994820
WBsf1016332
WBsf225967
Experimental_infoRNAi_result (13)
Expr_patternExpr3062
Expr4631
Expr4632
Expr6956
Expr1028843
Expr1035624
Expr1159723
Expr2009073
Expr2027309
Drives_constructWBCnstr00002376
WBCnstr00012135
WBCnstr00012136
Microarray_results (21)
Expression_cluster (118)
Interaction (172)
Map_infoMapIIIPosition20.9522Error0.053739
PositivePositive_cloneY39E4BInferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5286
Pseudo_map_position
ReferenceWBPaper00024370
WBPaper00028961
WBPaper00032322
WBPaper00038491
WBPaper00041771
WBPaper00046427
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