HNRNPU |
POU3F4 |
||
---|---|---|---|
Gene Name | heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A) | POU class 3 homeobox 4 | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 35 interactors: ACTB BTRC CASP3 CD5 CDKN2A CR2 ELL EP300 ERG GAS7 GRIN1 GRIN2D GTF2H1 HNRNPD HNRNPH3 IL7R KAT2B NDN NDRG1 NEDD4 NR3C1 PIN1 POLR2A POU3F4 PRMT1 PRPF40A PTPN11 SMN1 SREK1 STAU1 SYK TCERG1 WBP4 YAP1 ZNF689 | 4 interactors: HNRNPU POU3F1 POU3F2 POU3F3 | |
Entrez ID | 3192 | 5456 | |
HPRD ID | 04185 | 02076 | |
Ensembl ID | ENSG00000153187 | ENSG00000196767 | |
Uniprot IDs | Q00839 Q96BA7 | P49335 | |
PDB IDs | 1ZRJ | ||
Enriched GO Terms of Interacting Partners? |
|
|
|
Tagcloud ? | 17p13
1q21
1q44
2q23
2q31
agilent
annotations
asd
autism
backgrounds
cgh
cnv
cnvs
disabilities
dissect
encephalopathy
epileptic
exome
expand
hallux
implicates
infantile
intellectual
lissencephaly
mbd5
microcephaly
pafah1b1
pathogenicity
spasms
|
abnormality
accordingly
acgh
anomaly
asian
attempted
causative
counseling
de
deletions
dfnx2
ear
east
etiologic
homogeneity
iii
incomplete
inheritance
ip
korean
koreans
look
novo
partition
referral
sanger
siblings
striking
verify
|
|
Tagcloud (Difference) ? | 17p13
1q21
1q44
2q23
2q31
agilent
annotations
asd
autism
backgrounds
cgh
cnv
cnvs
disabilities
dissect
encephalopathy
epileptic
exome
expand
hallux
implicates
infantile
intellectual
lissencephaly
mbd5
microcephaly
pafah1b1
pathogenicity
spasms
|
abnormality
accordingly
acgh
anomaly
asian
attempted
causative
counseling
de
deletions
dfnx2
ear
east
etiologic
homogeneity
iii
incomplete
inheritance
ip
korean
koreans
look
novo
partition
referral
sanger
siblings
striking
verify
|
|
Tagcloud (Intersection) ? |