Gene Name |
heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A) |
heterogeneous nuclear ribonucleoprotein H3 (2H9) |
Image |
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No pdb structure |
Gene Ontology Annotations |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
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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
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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
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Entrez ID |
3192 |
3189 |
HPRD ID |
04185 |
03818 |
Ensembl ID |
ENSG00000153187
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ENSG00000096746
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Uniprot IDs |
Q00839
Q96BA7
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B4DHY1
P31942
Q53F48
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PDB IDs |
1ZRJ
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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
|
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Tagcloud (Intersection) ? |
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