HNRNPH3 |
HNRNPU |
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Gene Name | heterogeneous nuclear ribonucleoprotein H3 (2H9) | heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A) | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 26 interactors: ANXA11 C14orf1 C17orf85 CCL13 CHERP CRMP1 DDX17 DDX5 EEF1G ERG HNRNPA0 HNRNPA1 HNRNPD HNRNPF HNRNPH1 HNRNPU HNRNPUL1 IL7R KAT5 MAPK6 PIM2 RBM4 RPS4X TTR UTP14A ZMYM2 | 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 | |
Entrez ID | 3189 | 3192 | |
HPRD ID | 03818 | 04185 | |
Ensembl ID | ENSG00000096746 | ENSG00000153187 | |
Uniprot IDs | B4DHY1 P31942 Q53F48 | Q00839 Q96BA7 | |
PDB IDs | 1ZRJ | ||
Enriched GO Terms of Interacting Partners? |
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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
|
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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
|
||
Tagcloud (Intersection) ? |