COPB1 |
FOXB1 |
||
---|---|---|---|
Gene Name | coatomer protein complex, subunit beta 1 | forkhead box B1 | |
Image | No pdb structure | No pdb structure | |
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process |
|
||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 32 interactors: ADAM19 APP ARCN1 ARF1 COPE COPG1 COPG2 ERBB2IP FOXB1 GRB2 HLA-DPB1 HLA-G ID1 IRAK3 KCNK3 KDELR1 LZTS2 NUB1 PDGFRB PRKCE RGS2 RGS4 RHOQ SERTAD1 SNTA1 TANK TAPBP TMED10 TRIM37 UBQLN4 VPS18 XRCC6 | 8 interactors: COPB1 KRT31 KRT40 KRTAP10-3 KRTAP10-8 NOTCH2NL PHF5A TRIM27 | |
Entrez ID | 1315 | 27023 | |
HPRD ID | 02981 | 07017 | |
Ensembl ID | ENSG00000129083 | ENSG00000171956 | |
Uniprot IDs | P53618 | Q99853 | |
PDB IDs | |||
Enriched GO Terms of Interacting Partners? |
|
||
Tagcloud ? | ca037
ca530
cadd
chlamydiaceae
chlamydophila
copd1
copd2
inca
incc
pkn5
psittaci
scc1
scc2
scc3
sctc
sctd
sctj
sctl
sctn
sctq
sctr
scts
sctt
sctu
sctv
sctw
t3s
t3ss
tarp
|
15q22
box
commonly
de
deletions
disability
documented
epilepsy
familial
forkhead
genotype
intellectual
kb
larger
mb
microdeletions
narg2
narrowed
neighboring
neurologic
neurological
novo
origin
orphan
par
phenotype
region
rora
|
|
Tagcloud (Difference) ? | ca037
ca530
cadd
chlamydiaceae
chlamydophila
copd1
copd2
inca
incc
pkn5
psittaci
scc1
scc2
scc3
sctc
sctd
sctj
sctl
sctn
sctq
sctr
scts
sctt
sctu
sctv
sctw
t3s
t3ss
tarp
|
15q22
box
commonly
de
deletions
disability
documented
epilepsy
familial
forkhead
genotype
intellectual
kb
larger
mb
microdeletions
narg2
narrowed
neighboring
neurologic
neurological
novo
origin
orphan
par
phenotype
region
rora
|
|
Tagcloud (Intersection) ? |