Gene Name |
ankyrin repeat and SOCS box containing 6 |
transcription elongation factor B (SIII), polypeptide 1 (15kDa, elongin C) |
Image |
No pdb structure |
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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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- Attention deficit hyperactivity disorder ( 20732625)
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Protein-Protein Interactions |
6 interactors:
APP
FAM9B
L3MBTL3
RNF41
SH2B2
TCEB1
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34 interactors:
ASB6
CBX5
CENPC
COMMD1
CPTP
CUL2
CUL3
CUL5
CYP2J2
ECT2
EFNB3
GNB2L1
JTB
LRRC41
MCM7
MED8
METTL21C
MRAS
NOTCH4
PRAME
RCAN2
RNF7
SAT2
SERTAD1
SOCS1
SOCS3
SOCS6
TCEB2
TCEB3B
TCEB3C
USP33
VHL
WNT7B
ZYG11B
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Entrez ID |
140459 |
6921 |
HPRD ID |
10673 |
02875 |
Ensembl ID |
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ENSG00000154582
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Uniprot IDs |
Q9NWX5
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Q15369
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PDB IDs |
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1LM8
1LQB
1VCB
2C9W
2IZV
3DCG
3ZKJ
3ZRC
3ZRF
3ZTC
3ZTD
3ZUN
4AJY
4AWJ
4B95
4B9K
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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adrenal
arise
bc
chromaffin
cnl
copy
cul2
disrupting
elongin
enrichment
harbored
heterozygosity
hif1
hif1a
hippel
hypoxic
indeed
inherited
lindau
merit
normoxic
pcc
pheochromocytomas
predisposing
pseudohypoxic
rbx1
tceb2
vhl
von
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Tagcloud (Difference) ? |
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adrenal
arise
bc
chromaffin
cnl
copy
cul2
disrupting
elongin
enrichment
harbored
heterozygosity
hif1
hif1a
hippel
hypoxic
indeed
inherited
lindau
merit
normoxic
pcc
pheochromocytomas
predisposing
pseudohypoxic
rbx1
tceb2
vhl
von
|
Tagcloud (Intersection) ? |
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