Gene Name |
eukaryotic translation initiation factor 2, subunit 2 beta, 38kDa |
eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa |
Image |
No pdb structure |
No pdb structure |
Gene Ontology Annotations |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
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Protein-Protein Interactions |
22 interactors:
APLP1
APP
CCDC90B
CRMP1
CSNK2A1
CSNK2B
EIF2B1
EIF2B3
EIF2B4
EIF2B5
EIF2S1
EIF4G2
EIF5
HMGA1
KIAA1377
NCK1
PLEKHM1
PRKDC
TLE1
TP53
UNC119
ZBTB16
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5 interactors:
EIF2S1
EIF2S2
GOLM1
NDUFB8
STC2
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Entrez ID |
8894 |
8891 |
HPRD ID |
04882 |
09379 |
Ensembl ID |
ENSG00000125977
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ENSG00000070785
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Uniprot IDs |
P20042
Q6IBR8
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Q9HA31
Q9NR50
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PDB IDs |
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
biosynthetic
cd47
cycs
dataset
dj
e2f6
encyclopedia
extra
fmr1
fxr2
gpr37
logical
mapt
nrf1
paelr
park2
park6
park7
parkin
pen2
perturbation
pink1
psenen
retrieved
seq
stringent
tomm34
unrecognized
|
1090c
1980s
314a
318a
877c
ataxia
atrophy
compiled
deterioration
dystonic
genetics
hemiparesis
hereditary
leukoencephalopathy
list
macrocephaly
manifestation
matter
movements
necropsy
optic
spain
spasticity
suffered
vanishing
vwm
|
Tagcloud (Difference) ? |
biosynthetic
cd47
cycs
dataset
dj
e2f6
encyclopedia
extra
fmr1
fxr2
gpr37
logical
mapt
nrf1
paelr
park2
park6
park7
parkin
pen2
perturbation
pink1
psenen
retrieved
seq
stringent
tomm34
unrecognized
|
1090c
1980s
314a
318a
877c
ataxia
atrophy
compiled
deterioration
dystonic
genetics
hemiparesis
hereditary
leukoencephalopathy
list
macrocephaly
manifestation
matter
movements
necropsy
optic
spain
spasticity
suffered
vanishing
vwm
|
Tagcloud (Intersection) ? |
|