Description |
Bardet-Biedl syndrome 10 |
TNF superfamily member 11 |
Image |
No pdb structure |
|
GO Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
|
- Allergic disease (asthma, hay fever and/or eczema) (age of onset) ( 32603359)
- Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis) ( 32603359)
- Allergic rhinitis ( 30013184)
- Arthritis (juvenile idiopathic) ( 33106285)
- Asthma (childhood onset) ( 30929738)
- Bone mineral density ( 24249740 23437003)
- Bone mineral density (paediatric, total body less head) ( 24945404)
- Bone mineral density (paediatric, upper limb) ( 24945404)
- C-reactive protein levels ( 24763700)
- Cortical thickness ( 22792071)
- Crohn's disease ( 21102463)
- Heel bone mineral density ( 30598549)
- Lumbar spine bone mineral density (integral) ( 27476799)
- Lumbar spine bone mineral density (trabecular) ( 27476799)
- Serum alkaline phosphatase levels ( 33547301 29403010)
- Vitiligo ( 27723757)
|
Interacting Genes |
15 interacting genes:
CSNK1E
FRZB
GLIPR1
HDAC6
KRR1
MAP3K7
MAPK6
MAPK8IP2
NR4A1
PTK2
RASA1
RGS2
TM9SF3
TNFSF11
YAE1
|
32 interacting genes:
ADAM17
ADAM19
AKT1
BBS10
CEP126
DDAH2
EEF1A1
EZH2
LMO4
MAPK1
MAPK3
MAPK8
MBTPS1
MED24
MMP1
MMP3
MMP7
NFKB1
NFKBIA
OLFM4
PHAX
PLK1
PRXL2B
SBF1
SNRNP35
TMOD3
TNFRSF11A
TNFRSF11B
TRAF6
TRMT2A
UPK2
ZC3HC1
|
Entrez ID |
79738 |
8600 |
HPRD ID |
08036 |
04031 |
Ensembl ID |
ENSG00000179941
|
ENSG00000120659
|
Uniprot IDs |
Q8TAM1
|
O14788
Q54A98
Q5T9Y4
|
PDB IDs |
|
3URF
5BNQ
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
|
|
Tagcloud (Difference) ? |
|
|
Tagcloud (Intersection) ? |
|