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WormBase Tree Display for Gene: WBGene00002083

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Name Class

WBGene00002083SMapS_parentSequenceF57B9
IdentityVersion1
NameCGC_nameinf-1
Sequence_nameF57B9.6
Molecular_nameF57B9.6a
F57B9.6a.1
CE01341
F57B9.6b
CE38524
F57B9.6b.1
Other_nameCeIF
Ce1F
CELE_F57B9.6Accession_evidenceNDBBX284603
Public_nameinf-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classinf
Allele (27)
Legacy_information[C.elegansII] NMK. 1.7 kb RNA, encodes DEAD box RNA helicase, probable homolog of eukaryotic initiation factor 4A (71% identity to mouse eIF-4A). [Roussel and Bennett 1992; Seydoux and Fire 1994; KB]
RNASeq_FPKM (74)
GO_annotation (16)
Contained_in_operonCEOP3404
Ortholog (41)
Paralog (37)
Structured_descriptionConcise_descriptioninf-1 encodes a protein with high similarity to eukaryotic initiation factor 4A.Curator_confirmedWBPerson48
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable translation initiation factor activity. Predicted to be involved in cytoplasmic translational initiation. Predicted to be located in cytoplasmic stress granule. Expressed in germ line; intestine; and neurons. Is an ortholog of human EIF4A1 (eukaryotic translation initiation factor 4A1).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:0070512Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3284)
Molecular_infoCorresponding_CDSF57B9.6a
F57B9.6b
Corresponding_CDS_historyF57B9.6:wp142
Corresponding_transcriptF57B9.6a.1
F57B9.6b.1
Other_sequenceGR977793.1
FE918417.1
ES566650.1
ASC38606_1
EX913363.1
FG977831.1
DN557892.1
FG970769.1
FK806026.1
FC551428.1
FK803400.1
ES741404.1
GR977807.1
Dviv_contig12245
GR978817.1
MJ00509
TV00875
ES412913.1
FG979811.1
EX502582.1
PP00746
CGC00808_1
HSC00645_1
HGC09618_1
GR978045.1
EX007149.1
FG972190.1
CGC00446_1
GR367880.1
EY470060.1
MIC06954_1
TS00408
EX014451.1
Tcir_isotig32738
HC05057
FC817493.1
ES563429.1
MJC04507_1
EX012650.1
EX011990.1
ES566846.1
EX011264.1
TVC00105_1
MHC01966_1
AS10493
ES567366.1
FF681009.1
FF680508.1
SRC02952_1
FK806963.1
BQ804080.1
MH02374
FK808386.1
EX913923.1
ES739886.1
TS01431
LSC00686_1
ES743509.1
FG976723.1
GR978158.1
ES411217.1
FC812680.1
ES565842.1
EX913786.1
EY459200.1
TV00712
EX010328.1
HC01313
BUC01757_1
SR00911
CR01198
HBC26638_1
ASC02329_1
GO252454.1
PPC02577_1
Tcir_isotig18347
FC817810.1
FG970929.1
FE918404.1
EX014373.1
OVC00090
EX007716.1
EX012106.1
ACC09915_1
FK800056.1
MC01854
PSC04200_1
ES409110.1
FK803732.1
FG977961.1
FC818337.1
HS01413
HG02171
BQ804126.1
HBC02417_1
CBC00139_1
ES568333.1
FG971498.1
MI02063
BMC04046_1
PTC00722_1
FG587540.1
FF680066.1
DN557542.1
FC553033.1
Tcol_isotig23012
MCC00831_1
GW409372.1
FG971473.1
FG980543.1
EX911909.1
JK314780.1
AA294280.1
FK803745.1
ES744621.1
Associated_featureWBsf659131
WBsf659132
WBsf225171
WBsf225172
WBsf225173
WBsf225174
WBsf225175
Experimental_info (7)
Map_infoMapIIIPosition-0.894974Error0.001192
PositivePositive_cloneF57B9Inferred_automaticallyFrom sequence, transcript, pseudogene data
KB#LC2
Pseudo_map_position
Reference (11)
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