KCNQ2 |
ARIH2 |
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Gene Name | potassium channel, voltage gated KQT-like subfamily Q, member 2 | ariadne RBR E3 ubiquitin protein ligase 2 | |
Image | No pdb structure | No pdb structure | |
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 6 interactors: ARIH2 CALM1 CALM2 CALM3 KCNQ3 PRKCA | 44 interactors: ARAP1 BUB1 CBR3 CCDC33 CUL5 DISC1 DLST EEF1A1 EEF1G EML4 ENSA IL4R KAT5 KCNQ2 KIAA1377 LOC147791 NEDD8 PHF7 PPP2R1A PTN REL RHEB RPL8 SCAMP2 SGCE SLC1A6 TP53 TRIM27 UBE2D1 UBE2D2 UBE2D3 UBE2D4 UBE2E1 UBE2E2 UBE2E3 UBE2L3 UBE2L6 UBE2N UBE2R2 UBE2T UBE2V1 UGP2 UTP14A WDR91 | |
Entrez ID | 3785 | 10425 | |
HPRD ID | 03757 | 09286 | |
Ensembl ID | ENSG00000075043 | ENSG00000177479 | |
Uniprot IDs | O43526 Q4VXP7 Q53Y30 | O95376 Q6IBL8 | |
PDB IDs | |||
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | 16p12
2q24
5q14
9q34
aetiology
caln1
cdkl5
cgh
cnv
cnvs
counselling
ehmt1
encephalopathies
encompassing
epileptic
etiological
grin2a
hypsarrhythmia
infantile
intronic
iss
magi2
mef2c
microdeletions
microduplications
scn2a
spasms
stxbp1
xq28
|
aldo1
anxa2
cdna
cerebral
characterize
coding
cortical
ddit3
egr1
endoplasmic
ero1l
fold
gadd153
gas5
giig11
gpi1
hig1
hypoxia
microarray
ndr1
neuronal
p4hb
profiling
reinforce
repressed
reticulum
sac1p
ubiquitination
vdac2
|
|
Tagcloud (Difference) ? | 16p12
2q24
5q14
9q34
aetiology
caln1
cdkl5
cgh
cnv
cnvs
counselling
ehmt1
encephalopathies
encompassing
epileptic
etiological
grin2a
hypsarrhythmia
infantile
intronic
iss
magi2
mef2c
microdeletions
microduplications
scn2a
spasms
stxbp1
xq28
|
aldo1
anxa2
cdna
cerebral
characterize
coding
cortical
ddit3
egr1
endoplasmic
ero1l
fold
gadd153
gas5
giig11
gpi1
hig1
hypoxia
microarray
ndr1
neuronal
p4hb
profiling
reinforce
repressed
reticulum
sac1p
ubiquitination
vdac2
|
|
Tagcloud (Intersection) ? |