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WormBase Tree Display for Gene: WBGene00012950

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Name Class

WBGene00012950SMapS_parentSequenceY47H9C
IdentityVersion2
NameCGC_nameeif-2BbetaPerson_evidenceWBPerson2266
Sequence_nameY47H9C.7
Molecular_nameY47H9C.7
Y47H9C.7.1
CE20267
Other_nameCELE_Y47H9C.7Accession_evidenceNDBBX284601
Public_nameeif-2Bbeta
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:54WBPerson1971EventImportedInitial conversion from CDS class of WS125
209 Jan 2017 15:00:31WBPerson2970Name_changeCGC_nameeif-2Bbeta
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classeif
Allele (61)
RNASeq_FPKM (74)
GO_annotation00103346
00103347
00103348
00103349
00103350
00103351
00119917
Ortholog (37)
ParalogWBGene00007236Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008670Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00014221Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionY47H9C.7 is orthologous to the human gene EUKARYOTIC TRANSLATION INITIATION FACTOR 2B, SUBUNIT 2 (BETA, 39KD) (EIF2B2; OMIM:606454), which when mutated leads to disease.Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated06 Aug 2004 00:00:00
Automated_descriptionPredicted to enable translation initiation factor activity. Predicted to contribute to guanyl-nucleotide exchange factor activity. Predicted to be involved in translational initiation. Predicted to be part of eukaryotic translation initiation factor 2B complex. Human ortholog(s) of this gene implicated in leukoencephalopathy with vanishing white matter 2. Is an ortholog of human EIF2B2 (eukaryotic translation initiation factor 2B subunit beta).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:0070373Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3258)
DOID:0060868Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3258)
Molecular_infoCorresponding_CDSY47H9C.7
Corresponding_transcriptY47H9C.7.1
Other_sequenceMH07180
HBC04511_1
ES408816.1
Hbac_isotig02304
Oden_isotig10408
Acan_isotig15230
Oden_isotig10407
FK800800.1
Tcol_isotig10627
CBC10110_1
Associated_featureWBsf649638
WBsf220374
Experimental_infoRNAi_result (26)
Expr_patternExpr1014092
Expr1035743
Expr1160303
Expr2011244
Expr2029480
Microarray_results (19)
Expression_cluster (98)
Interaction (87)
Map_infoPositivePositive_cloneY47H9CInferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionI12.9065
ReferenceWBPaper00027281
WBPaper00038491
WBPaper00055090
WBPaper00064339
MethodGene