Gene Name |
general transcription factor IIB |
forkhead box F2 |
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 |
56 interactors:
ATF4
BCL3
CIITA
CREBBP
CTBP1
DEPDC7
DHX9
DRAP1
EP300
ESR1
ESRRA
FBXO25
FOXF2
GTF2E1
GTF2E2
GTF2F1
GTF2F2
GTF2H4
HMGCL
HNF4A
HSF1
IKZF1
JAK3
JUN
KLF5
MCM2
MECP2
MYC
NCOA1
NCOA3
NCOA4
NCOR1
NOLC1
NR1D2
NR2F1
NR5A1
POLR2A
POLR2E
POU3F2
PSMC2
PSMC5
REL
RELA
REST
SLC22A2
SRA1
TAF11
TAF9
TBP
TBPL1
TCEA2
THRA
TNIP1
TRAM2
VDR
YWHAE
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2 interactors:
GTF2B
TBP
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Entrez ID |
2959 |
2295 |
HPRD ID |
08928 |
09131 |
Ensembl ID |
ENSG00000137947
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ENSG00000137273
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Uniprot IDs |
Q00403
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Q12947
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PDB IDs |
1C9B
1DL6
1RLY
1RO4
1TFB
1VOL
2PHG
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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6p22
6pter
anomalies
atxn1
banding
cgh
dek
der
detachment
e2f3
edn1
forkhead
foxc1
foxq1
girl
gtg
hyperplastic
newborn
nrn1
nrns1
p22
phpv
pter
q1
retardation
sky
trisomy
vitreous
xx
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Tagcloud (Difference) ? |
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6p22
6pter
anomalies
atxn1
banding
cgh
dek
der
detachment
e2f3
edn1
forkhead
foxc1
foxq1
girl
gtg
hyperplastic
newborn
nrn1
nrns1
p22
phpv
pter
q1
retardation
sky
trisomy
vitreous
xx
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Tagcloud (Intersection) ? |
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