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WormBase Tree Display for Gene: WBGene00001169

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Name Class

WBGene00001169SMapS_parentSequenceCHROMOSOME_X
IdentityVersion2
NameCGC_nameeef-1A.2Person_evidenceWBPerson1787
WBPerson10190
Sequence_nameR03G5.1
Molecular_nameR03G5.1
R03G5.1.1
CE01270
R03G5.1.2
R03G5.1.3
Other_nameeln-2
eft-4
C54D2.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
R03G5.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
R03G5.bCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_R03G5.1Accession_evidenceNDBBX284606
Public_nameeef-1A.2
DB_infoDatabaseAceViewgeneXI443
WormQTLgeneWBGene00001169
WormFluxgeneWBGene00001169
NDBlocus_tagCELE_R03G5.1
NCBIgene181044
RefSeqproteinNM_076922.5
SwissProtUniProtAccP53013
UniProt_GCRPUniProtAccP53013
OMIMgene602959
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
203 Aug 2010 09:32:43WBPerson2970Name_changeCGC_nameeef-1A-2
Other_nameeft-4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classeef
Allele (48)
Legacy_information[C.elegansII] NMK. Encodes EF1 alpha protein, aa sequence identical to eft-3. [FK]
RNASeq_FPKM (74)
GO_annotation00108369
00108370
00108371
00108372
Ortholog (50)
Paralog (17)
Structured_descriptionConcise_descriptioneef-1A.2 encodes a translation elongation factor 1-alpha homolog that is required for embryonic viability, fertility, and a normal postembryonic growth rate; eef-1A.2 encodes at least one alternatively spliced coding sequence identical to that of eef-1A.1.Paper_evidenceWBPaper00004313
WBPaper00004540
WBPaper00005654
Curator_confirmedWBPerson48
WBPerson1843
WBPerson567
Date_last_updated03 Dec 2014 00:00:00
Automated_descriptionPredicted to enable GTP binding activity; GTPase activity; and translation elongation factor activity. Predicted to be involved in translational elongation. Human ortholog(s) of this gene implicated in Alzheimer's disease; autosomal dominant intellectual developmental disorder 38; developmental and epileptic encephalopathy 33; and ovarian cancer. Is an ortholog of human EEF1A1 (eukaryotic translation elongation factor 1 alpha 1); EEF1A1P5 (eukaryotic translation elongation factor 1 alpha 1 pseudogene 5); and EEF1A2 (eukaryotic translation elongation factor 1 alpha 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:3192)
DOID:0070068Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3192)
DOID:0080463Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3192)
DOID:2394Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3192)
Molecular_infoCorresponding_CDSR03G5.1
Corresponding_CDS_historyR03G5.1b:wp272
R03G5.1c:wp272
R03G5.1d:wp162
R03G5.1d:wp272
Corresponding_transcriptR03G5.1.1
R03G5.1.2
R03G5.1.3
Other_sequence (769)
Associated_feature (21)
Experimental_infoRNAi_result (30)
Expr_patternExpr1030746
Expr1154893
Expr2011178
Expr2029414
Drives_construct (11)
Construct_productWBCnstr00037980
Microarray_results (34)
Expression_cluster (226)
Interaction (307)
Map_infoMapXPosition-1.12456
PositivePositive_cloneR03G5Inferred_automaticallyFrom sequence, transcript, pseudogene data
YO#EFG5
Pseudo_map_position
ReferenceWBPaper00024924
WBPaper00025088
WBPaper00027281
WBPaper00037777
WBPaper00038491
WBPaper00049828
WBPaper00055090
WBPaper00065634
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