8672


Homo sapiens (NCBI)

Features
Gene ID: 8672
  
Biological name :
  
Synonyms : EIF4G3 / eIF-4G 3|eIF4G 3|eIF4GII / eukaryotic translation initiation factor 4 gamma 3
  
Possible biological names infered from orthology :
  
Species: Homo sapiens (NCBI)
  
Chr. number:
Strand:
Band:
Gene start:
Gene end:
  
Corresponding Affymetrix probe sets: 1554309_at (Human Genome U133 Plus 2.0 Array)   1554310_a_at (Human Genome U133 Plus 2.0 Array)   201935_s_at (Human Genome U133 Plus 2.0 Array)   201936_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: RefSeq - 1034562996
RefSeq - 1034562914
RefSeq - 1034562917
RefSeq - 1034562919
RefSeq - 1034562921
RefSeq - 1034562923
RefSeq - 1034562925
RefSeq - 1034562927
RefSeq - 1034562930
RefSeq - 1034562934
RefSeq - 1034562936
RefSeq - 1034562938
RefSeq - 1034562940
RefSeq - 1034562942
RefSeq - 1034562944
RefSeq - 1034562946
RefSeq - 1034562950
RefSeq - 1034562952
RefSeq - 1034562954
RefSeq - 1034562956
RefSeq - 1034562959
RefSeq - 1034562961
RefSeq - 1034562963
RefSeq - 1034562965
RefSeq - 1034562967
RefSeq - 1034562969
RefSeq - 1034562971
RefSeq - 1034562973
RefSeq - 1034562975
RefSeq - 1034562977
RefSeq - 1034562979
RefSeq - 1034562981
RefSeq - 1034562983
RefSeq - 1034562985
RefSeq - 1034562987
RefSeq - 1034562989
RefSeq - 1034562991
RefSeq - 1034562994
RefSeq - 10092601
RefSeq - 1370455054
RefSeq - 311771714
RefSeq - 311771716
RefSeq - 311771718
RefSeq - 767906566
RefSeq - 767906576
RefSeq - 767906594
RefSeq - 767906596
RefSeq - 767906602
RefSeq - 767906604
RefSeq - 767906616
RefSeq - NC_000001.11
RefSeq - NG_047026.1
RefSeq - NP_001185730.1
RefSeq - NP_001185731.1
RefSeq - NP_001185732.1
RefSeq - NP_003751.2
RefSeq - XP_011540658.1
RefSeq - XP_011540663.1
RefSeq - XP_011540672.1
RefSeq - XP_011540673.1
RefSeq - XP_011540676.1
RefSeq - XP_011540677.1
RefSeq - XP_011540683.1
RefSeq - XP_016858161.1
RefSeq - XP_016858162.1
RefSeq - XP_016858163.1
RefSeq - XP_016858164.1
RefSeq - XP_016858165.1
RefSeq - XP_016858166.1
RefSeq - XP_016858167.1
RefSeq - XP_016858168.1
RefSeq - XP_016858170.1
RefSeq - XP_016858171.1
RefSeq - XP_016858172.1
RefSeq - XP_016858173.1
RefSeq - XP_016858174.1
RefSeq - XP_016858175.1
RefSeq - XP_016858176.1
RefSeq - XP_016858178.1
RefSeq - XP_016858179.1
RefSeq - XP_016858180.1
RefSeq - XP_016858181.1
RefSeq - XP_016858182.1
RefSeq - XP_016858183.1
RefSeq - XP_016858184.1
RefSeq - XP_016858185.1
RefSeq - XP_016858186.1
RefSeq - XP_016858187.1
RefSeq - XP_016858188.1
RefSeq - XP_016858189.1
RefSeq - XP_016858190.1
RefSeq - XP_016858191.1
RefSeq - XP_016858192.1
RefSeq - XP_016858193.1
RefSeq - XP_016858194.1
RefSeq - XP_016858195.1
RefSeq - XP_016858196.1
RefSeq - XP_016858197.1
RefSeq - XP_016858198.1
RefSeq - XP_016858199.1
RefSeq - XP_016858200.1
RefSeq - XP_024306301.1
RefSeq - XM_017002709.2
RefSeq - XM_017002710.2
RefSeq - NM_001198801.1
RefSeq - NM_001198802.1
RefSeq - NM_001198803.2
RefSeq - NM_003760.4
RefSeq - XM_017002711.2
RefSeq - XM_024450533.1
RefSeq - XR_002957947.1
RefSeq - XR_002957948.1
RefSeq - XM_011542356.3
RefSeq - XM_011542361.3
RefSeq - XM_011542370.2
RefSeq - XM_011542371.2
RefSeq - XM_011542374.2
RefSeq - XM_011542375.3
RefSeq - XM_011542381.3
RefSeq - XM_017002672.2
RefSeq - XM_017002673.2
RefSeq - XM_017002674.2
RefSeq - XM_017002675.2
RefSeq - XM_017002676.2
RefSeq - XM_017002677.2
RefSeq - XM_017002678.2
RefSeq - XM_017002679.2
RefSeq - XM_017002681.2
RefSeq - XM_017002682.2
RefSeq - XM_017002683.2
RefSeq - XM_017002684.2
RefSeq - XM_017002685.2
RefSeq - XM_017002686.2
RefSeq - XM_017002687.2
RefSeq - XM_017002689.2
RefSeq - XM_017002690.2
RefSeq - XM_017002691.2
RefSeq - XM_017002692.2
RefSeq - XM_017002693.2
RefSeq - XM_017002694.2
RefSeq - XM_017002695.2
RefSeq - XM_017002696.2
RefSeq - XM_017002697.2
RefSeq - XM_017002698.2
RefSeq - XM_017002699.2
RefSeq - XM_017002700.2
RefSeq - XM_017002701.2
RefSeq - XM_017002702.2
RefSeq - XM_017002703.2
RefSeq - XM_017002704.2
RefSeq - XM_017002705.2
RefSeq - XM_017002706.2
RefSeq - XM_017002707.2
RefSeq - XM_017002708.2
  
See co-cited genes in PubMed
Warning: Please see the Ensembl gene model ENSG00000075151 to get all the annotations available for this gene.


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006413 translational initiation IEA
 biological_processGO:0006446 regulation of translational initiation TAS
 biological_processGO:0010507 negative regulation of autophagy IMP
 biological_processGO:0016032 viral process IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0016281 eukaryotic translation initiation factor 4F complex TAS
 molecular_functionGO:0000339 RNA cap binding IEA
 molecular_functionGO:0003723 RNA binding HDA
 molecular_functionGO:0003729 mRNA binding IBA
 molecular_functionGO:0003743 translation initiation factor activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008135 translation factor activity, RNA binding TAS


Pathways (from Reactome)
Pathway description
No match


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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