Gene Name |
euchromatic histone-lysine N-methyltransferase 1 |
pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha |
Image |
|
No pdb structure |
Gene Ontology Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
|
|
Protein-Protein Interactions |
12 interactors:
ATXN1
DNMT3A
EED
EZH2
HIST1H3A
HIST3H3
LZTR1
PCBD1
TP53
TRIM15
UBC
WIZ
|
49 interactors:
ACIN1
APP
BRD7
CACNA1C
CALCOCO1
CDK5RAP2
CEBPZ
DENND4A
DIP2C
DVL2
DYRK1B
EHMT1
FXR2
GORASP2
GTF3C3
HES4
HNF1A
HNF1B
HNF4A
KLF13
LNX1
MIS18BP1
NFKB1
NIF3L1
NUDT18
PAH
PAPOLG
PCBD2
POLR3A
RBL2
RPS24
SAP30
SCMH1
SMARCD1
SOWAHC
SUPT5H
TFF3
TIMELESS
TRIM5
WDYHV1
WWP1
ZBTB25
ZNF195
ZNF202
ZNF23
ZNF263
ZNF451
ZNF567
ZNF714
|
Entrez ID |
79813 |
5092 |
HPRD ID |
07383 |
00523 |
Ensembl ID |
ENSG00000181090
|
ENSG00000166228
|
Uniprot IDs |
Q9H9B1
|
P61457
|
PDB IDs |
2IGQ
2RFI
3B7B
3B95
3FPD
3HNA
3MO0
3MO2
3MO5
3SW9
3SWC
4I51
|
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
16p12
2q24
5q14
9q34
aetiology
caln1
cdkl5
cgh
cnv
cnvs
counselling
encephalopathies
encompassing
epileptic
etiological
grin2a
hypsarrhythmia
infantile
intronic
iss
kcnq2
magi2
mef2c
microdeletions
microduplications
scn2a
spasms
stxbp1
xq28
|
|
Tagcloud (Difference) ? |
16p12
2q24
5q14
9q34
aetiology
caln1
cdkl5
cgh
cnv
cnvs
counselling
encephalopathies
encompassing
epileptic
etiological
grin2a
hypsarrhythmia
infantile
intronic
iss
kcnq2
magi2
mef2c
microdeletions
microduplications
scn2a
spasms
stxbp1
xq28
|
|
Tagcloud (Intersection) ? |
|