Gene Name |
heterogeneous nuclear ribonucleoprotein F |
RNA binding protein, fox-1 homolog (C. elegans) 1 |
Image |
|
|
Gene Ontology Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
|
|
Protein-Protein Interactions |
33 interactors:
AES
C1orf94
CCDC33
DZIP3
EIF4ENIF1
ERG
HNRNPA0
HNRNPD
HNRNPH1
HNRNPH3
HNRNPM
HNRNPUL1
HSFY1
IKZF3
NCBP1
NCBP2
NDRG1
POLR2A
PRPF40A
RBFOX1
RBFOX2
RBM4
SF1
SF3B4
SNRPC
SUMO4
TFG
TGM2
TOE1
TXNL4A
VAV2
YWHAQ
ZNF689
|
33 interactors:
ALG13
ATN1
ATXN1
ATXN2
BHLHE40
C1orf94
CELF3
CRX
DAB1
DAZAP2
DMRTB1
DVL2
FAM168A
GCA
HNRNPF
HSFX1
HSFY1
KIFAP3
LZTS2
MAGED1
NOC2L
NUMBL
PCBP4
PRR20A
PRRC2A
PSMF1
QKI
RBFOX2
RBM24
RBPMS
RHOXF2
SNRPN
TNIP1
|
Entrez ID |
3185 |
54715 |
HPRD ID |
03023 |
16091 |
Ensembl ID |
ENSG00000169813
|
ENSG00000078328
|
Uniprot IDs |
P52597
|
B7Z1U7
F5H0M1
Q59HD3
Q9NWB1
|
PDB IDs |
2HGL
2HGM
2HGN
2KFY
2KG0
2KG1
3TFY
|
2ERR
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
|
16p13
2p13
3p13
abat
anomalies
cgh
cytogenetic
determining
difficulties
disability
duplicated
duplication
duplications
dysmorphisms
epilepsy
facial
girl
grin2a
hotspot
intellectual
litaf
microdeletions
novo
omim
overlapping
pmm2
spanning
tmem114
vertebral
|
Tagcloud (Difference) ? |
|
16p13
2p13
3p13
abat
anomalies
cgh
cytogenetic
determining
difficulties
disability
duplicated
duplication
duplications
dysmorphisms
epilepsy
facial
girl
grin2a
hotspot
intellectual
litaf
microdeletions
novo
omim
overlapping
pmm2
spanning
tmem114
vertebral
|
Tagcloud (Intersection) ? |
|