WormBase Tree Display for Gene: WBGene00002083
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WBGene00002083 | SMap | S_parent | Sequence | F57B9 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 1 | |||||||
Name | CGC_name | inf-1 | |||||||
Sequence_name | F57B9.6 | ||||||||
Molecular_name | F57B9.6a | ||||||||
F57B9.6a.1 | |||||||||
CE01341 | |||||||||
F57B9.6b | |||||||||
CE38524 | |||||||||
F57B9.6b.1 | |||||||||
Other_name | CeIF | ||||||||
Ce1F | |||||||||
CELE_F57B9.6 | Accession_evidence | NDB | BX284603 | ||||||
Public_name | inf-1 | ||||||||
DB_info | Database (12) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 07 Apr 2004 11:29:26 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | inf | ||||||||
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_operon | CEOP3404 | ||||||||
Ortholog (41) | |||||||||
Paralog (37) | |||||||||
Structured_description | Concise_description | inf-1 encodes a protein with high similarity to eukaryotic initiation factor 4A. | Curator_confirmed | WBPerson48 | |||||
Date_last_updated | 17 Jun 2004 00:00:00 | ||||||||
Automated_description | Predicted 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_evidence | WBPaper00065943 | ||||||
Curator_confirmed | WBPerson324 | ||||||||
WBPerson37462 | |||||||||
Inferred_automatically | This description was generated automatically by a script based on data from the WS291 version of WormBase | ||||||||
Date_last_updated | 29 Nov 2023 00:00:00 | ||||||||
Disease_info | Potential_model | DOID:0070512 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3284) | ||||
Molecular_info | Corresponding_CDS | F57B9.6a | |||||||
F57B9.6b | |||||||||
Corresponding_CDS_history | F57B9.6:wp142 | ||||||||
Corresponding_transcript | F57B9.6a.1 | ||||||||
F57B9.6b.1 | |||||||||
Other_sequence | GR977793.1 | ||||||||
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_feature | WBsf659131 | ||||||||
WBsf659132 | |||||||||
WBsf225171 | |||||||||
WBsf225172 | |||||||||
WBsf225173 | |||||||||
WBsf225174 | |||||||||
WBsf225175 | |||||||||
Experimental_info (7) | |||||||||
Map_info | Map | III | Position | -0.894974 | Error | 0.001192 | |||
Positive | Positive_clone | F57B9 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
KB#LC2 | |||||||||
Pseudo_map_position | |||||||||
Reference (11) | |||||||||
Remark | Map 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 | |||||||
Method | Gene |