ZBTB8A |
FXR2 |
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Gene Name | zinc finger and BTB domain containing 8A | fragile X mental retardation, autosomal homolog 2 | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 51 interactors: AEN AP1M1 AP2M1 ARMCX1 BAZ2B BYSL CCDC33 CDKL3 CEP70 DDX6 DVL2 EIF1AD EP300 FAM161A FXR2 GPATCH2L KAT5 KAT7 KIF5B KIF9 KIFC3 LMO3 LNX1 MCM10 MFAP1 MYO15B PAXIP1 PIAS2 PRKAA2 PSMC1 RAD23A RPL9 SDCBP SYT6 TNIP3 TRIM41 UBE2I WDYHV1 YES1 ZBTB24 ZBTB48 ZBTB49 ZCCHC10 ZGPAT ZMAT2 ZNF138 ZNF250 ZNF276 ZNF408 ZNF417 ZNF587 | 90 interactors: AMOTL2 AP1M1 AP2M1 ARL6IP1 BAZ2B BRCA1 BYSL C10orf62 C1orf35 CALCOCO2 CAMK2D CBS CCDC33 CCDC85B CDKL3 CEP44 CEP55 COIL CYFIP1 CYFIP2 DPPA2 EWSR1 FAM90A1 FBP1 FMR1 FTH1 FXR1 GKAP1 HMBOX1 HNRNPC KCNRG KCTD4 KIAA1217 KIF1A KRT20 KXD1 LASP1 LCMT1 LCP2 LDOC1 MBIP MCRS1 MEAF6 MFAP1 MIA3 MORF4L1 MRPL43 NCK2 NDN NECAB2 NIF3L1 NME1 NONO NT5C2 PAF1 PAICS PCBD1 PIM1 POM121 PRAM1 PSME3 PTS RABAC1 RALYL RBBP8 RBMX RBPMS RPIA RTN3 RTN4 SCEL SNAP23 SRPK2 SSSCA1 SYT6 SYTL4 TBC1D22B THAP1 TNNT1 TRAF2 TRIM23 TRIM29 TRIM37 TSC22D4 YES1 ZBTB22 ZBTB8A ZMAT2 ZNF451 ZSCAN1 | |
Entrez ID | 653121 | 9513 | |
HPRD ID | 18902 | 05629 | |
Ensembl ID | ENSG00000160062 | ENSG00000129245 | |
Uniprot IDs | D3DPQ1 Q96BR9 | P51116 | |
PDB IDs | 3H8Z | ||
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | acting
boxes
bozf
bozf1
c2h2
cdkn1a
cervix
competed
concentrated
finger
fingers
gc
interacted
kruppel
oncogenesis
oncoprotein
p21waf
paired
pok
poz
proto
proximal
repress
repressed
sp1
speckles
stimulates
zinc
|
17p13
adipocytes
array
cgh
disability
duplication
dysmorphic
encodes
encompassing
facial
fingers
fissures
glut4
hyperpigmentation
intellectual
mandible
nlgn2
nostrils
obesity
p13
palpebral
proposita
recognizable
referred
seizures
slc2a4
slender
tp53
upturned
|
|
Tagcloud (Difference) ? | acting
boxes
bozf
bozf1
c2h2
cdkn1a
cervix
competed
concentrated
finger
gc
interacted
kruppel
oncogenesis
oncoprotein
p21waf
paired
pok
poz
proto
proximal
repress
repressed
sp1
speckles
stimulates
zinc
|
17p13
adipocytes
array
cgh
disability
duplication
dysmorphic
encodes
encompassing
facial
fissures
glut4
hyperpigmentation
intellectual
mandible
nlgn2
nostrils
obesity
p13
palpebral
proposita
recognizable
referred
seizures
slc2a4
slender
tp53
upturned
|
|
Tagcloud (Intersection) ? | fingers
|