EHMT1 |
WIZ |
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Gene Name | euchromatic histone-lysine N-methyltransferase 1 | widely interspaced zinc finger motifs | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process |
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Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 12 interactors: ATXN1 DNMT3A EED EZH2 HIST1H3A HIST3H3 LZTR1 PCBD1 TP53 TRIM15 UBC WIZ | 14 interactors: C8orf33 CDKN1A EHMT1 EHMT2 OSGEP PIN1 RCC1 RPP14 RPS10 SMN1 SUV39H1 SUV39H2 TK1 TSC22D1 | |
Entrez ID | 79813 | 58525 | |
HPRD ID | 07383 | 11686 | |
Ensembl ID | ENSG00000181090 | ENSG00000011451 | |
Uniprot IDs | Q9H9B1 | B3KVH1 M0QXA7 O95785 | |
PDB IDs | 2IGQ 2RFI 3B7B 3B95 3FPD 3HNA 3MO0 3MO2 3MO5 3SW9 3SWC 4I51 | ||
Enriched GO Terms of Interacting Partners? |
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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
|
ankyrin
asd
autism
autistic
ba21
ba40
boundaries
brodmann
delays
dimethylation
dorn
ehmt1
ehmt2
g9a
glp
h3k9
heteromeric
intellectual
kleefstra
lys968arg
methyltransferases
nonsynonymous
novelty
postmortem
prioritized
raphe
restrictive
surmise
thr961ile
|
|
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
|
ankyrin
asd
autism
autistic
ba21
ba40
boundaries
brodmann
delays
dimethylation
dorn
ehmt2
g9a
glp
h3k9
heteromeric
intellectual
kleefstra
lys968arg
methyltransferases
nonsynonymous
novelty
postmortem
prioritized
raphe
restrictive
surmise
thr961ile
|
|
Tagcloud (Intersection) ? | ehmt1
|