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  2. EIF4G2 - eukaryotic translation initiation factor 4 gamma 2 Gene

EIF4G2 - eukaryotic translation initiation factor 4 gamma 2 Gene

Homo sapiens

Also known as P97; AAG1; DAP5; NAT1

Gene ID: 1982 | Gene type: protein coding

About EIF4G2

Cytogenetic location: 11p15.4 Genomic coordinates (GRCh38): 11:10,797,046-10,808,926 (from NCBI)

This gene has 31 transcripts (splice variants), 280 orthologues and 2 paralogues. Ubiquitous expression in thyroid (RPKM 207.4), placenta (RPKM 201.0) and 25 other tissues.

Summary

Translation initiation is mediated by specific recognition of the cap structure by eukaryotic translation initiation factor 4F (eIF4F), which is a cap binding protein complex that consists of three subunits: eIF4A, eIF4E and eIF4G. The protein encoded by this gene shares similarity with the C-terminal region of eIF4G that contains the binding sites for eIF4A and eIF3; eIF4G, in addition, contains a binding site for eIF4E at the N-terminus. Unlike eIF4G, which supports cap-dependent and independent translation, this gene product functions as a general repressor of translation by forming translationally inactive complexes. In vitro and in vivo studies indicate that translation of this mRNA initiates exclusively at a non-AUG (GUG) codon. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008]

EIF4G2 Products(3)

mRNA Protein Name
NM_001042559.3 NP_001036024.3 eukaryotic translation initiation factor 4 gamma 2 isoform 2
NM_001172705.1 NP_001166176.1 eukaryotic translation initiation factor 4 gamma 2 isoform 1
NM_001418.4 NP_001409.3 eukaryotic translation initiation factor 4 gamma 2 isoform 1

EIF4G2 Protein Structure

MIF4G

MIF4G: MIF4G domain (79 - 307)

MA3

MA3: MA3 domain (548 - 655)

W2

W2: eIF4-gamma/eIF5/eIF2-epsilon (825 - 905)

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  • 907 a.a.
Protein Preferred Names Protein Names

eukaryotic translation initiation factor 4 gamma 2

DAP-5

Related Diseases

Diseases Alias
Mouth Disease

Mouth Diseases

Mouth Disorders

Amyotrophic Lateral Sclerosis 1

Amyotrophic Lateral Sclerosis

ALS

Lou Gehrig Disease

Amyotrophic Lateral Sclerosis Type 1

Charcot Disease

ALS1

Amyotrophic Lateral Sclerosis, Susceptibility To

Fals

Lou Gehrig'S Disease

Mnd

Motor Neuron Disease

Familial Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis 1, Familial

Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

Motor Neuron Disease, Bulbar

Motor Neurone Disease

Amyotrophic Lateral Sclerosis With Dementia

Dementia With Amyotrophic Lateral Sclerosis

Motor Neuron Disease, Amyotrophic Lateral Sclerosis

Sclerosis, Lateral, Amyotrophic

Sclerosis, Lateral, Amyotrophic, Type 1

Amyotrophic Sclerosis

Als - [Amyotrophic Lateral Sclerosis]

Wasting Palsy

Amyotrophic Paralysis

Amyotrophy Lateral Sclerosis

Wasting Paralysis

Spinal Progressive Amyotrophy

Progressive Atrophic Paralysis

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus EIF4G2 MGD MGI:109207
Rattus norvegicus EIF4G2 RGD RGD:1305294
Bos taurus EIF4G2 VGNC VGNC:28416
Macaca mulatta EIF4G2 VGNC VGNC:72196
Felis catus EIF4G2 VGNC VGNC:61795
Canis familiaris EIF4G2 VGNC VGNC:52256