Gene Name |
stanniocalcin 2 |
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 |
11 interactors:
ADAM11
AIFM1
ARHGEF40
ARRB2
CARHSP1
EIF2B3
PEBP1
POLR2C
POLR3F
PPP1R8
PTN
|
5 interactors:
EIF2S1
EIF2S2
GOLM1
NDUFB8
STC2
|
Entrez ID |
8614 |
8891 |
HPRD ID |
04717 |
09379 |
Ensembl ID |
ENSG00000113739
|
ENSG00000070785
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Uniprot IDs |
O76061
Q6FHC9
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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 ? |
alleviate
altering
alternating
american
capillaries
ccl2
closer
coat
concave
convex
dawley
diepoxide
endometrium
eosin
follicles
ginseng
glands
hematoxylin
nell1
ovarian
pappa
pla2g4a
pof
premature
sprague
uterine
vcd
vinylcyclohexene
visible
|
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) ? |
alleviate
altering
alternating
american
capillaries
ccl2
closer
coat
concave
convex
dawley
diepoxide
endometrium
eosin
follicles
ginseng
glands
hematoxylin
nell1
ovarian
pappa
pla2g4a
pof
premature
sprague
uterine
vcd
vinylcyclohexene
visible
|
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) ? |
|