EIF2B2 (eukaryotic translation initiation factor 2B subunit beta)

2014-11-01  

Identity

HGNC
LOCATION
14q24.3
LOCUSID
ALIAS
EIF-2Bbeta,EIF2B
FUSION GENES

Other Information

Locus ID:

NCBI: 8892
MIM: 606454
HGNC: 3258
Ensembl: ENSG00000119718

Variants:

dbSNP: 8892
ClinVar: 8892
TCGA: ENSG00000119718
COSMIC: EIF2B2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000119718ENST00000266126P49770
ENSG00000119718ENST00000266126Q53XC2
ENSG00000119718ENST00000553401H0YJJ8
ENSG00000119718ENST00000554748H0YK01
ENSG00000119718ENST00000556028G3V5E5

Expression (GTEx)

0
5
10
15
20
25
30
35
40

Pathways

PathwaySourceExternal ID
RNA transportKEGGko03013
RNA transportKEGGhsa03013
Metabolism of proteinsREACTOMER-HSA-392499
TranslationREACTOMER-HSA-72766
Eukaryotic Translation InitiationREACTOMER-HSA-72613
Cap-dependent Translation InitiationREACTOMER-HSA-72737
Recycling of eIF2:GDPREACTOMER-HSA-72731
Gene ExpressionREACTOMER-HSA-74160

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
333348792021Mutational analysis of the alpha subunit of eIF2B provides insights into the role of eIF2B bodies in translational control and VWM disease.2
333348792021Mutational analysis of the alpha subunit of eIF2B provides insights into the role of eIF2B bodies in translational control and VWM disease.2
280417992017eIF2B-related multisystem disorder in two sisters with atypical presentations.0
290364342017Novel mechanisms of eIF2B action and regulation by eIF2α phosphorylation.33
280417992017eIF2B-related multisystem disorder in two sisters with atypical presentations.0
290364342017Novel mechanisms of eIF2B action and regulation by eIF2α phosphorylation.33
227295082013Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course.1
227295082013Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course.1
222853772012Vanishing white matter disease caused by EIF2B2 mutation with the presentation of an adrenoleukodystrophy phenotype.1
222853772012Vanishing white matter disease caused by EIF2B2 mutation with the presentation of an adrenoleukodystrophy phenotype.1
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.15
207340642010A large-scale candidate gene association study of age at menarche and age at natural menopause.57
206280862010Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.15
207340642010A large-scale candidate gene association study of age at menarche and age at natural menopause.57
199131212009Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.105

Citation

Dessen P

EIF2B2 (eukaryotic translation initiation factor 2B subunit beta)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/62774