FXR2 |
THAP1 |
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Gene Name | fragile X mental retardation, autosomal homolog 2 | THAP domain containing, apoptosis associated protein 1 | |
Image | |||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 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 | 58 interactors: ACOT7 AKAP17A AKAP9 AP2B1 ARL6IP4 BAG5 BMS1P5 BYSL C11orf57 C1orf35 C7orf50 CHD2 CSNK2A1 DCAF8 DVL2 FAM124A FAM133A FXR2 GPATCH2L HNRNPLL KLF12 KRTAP10-7 LASP1 MORF4L1 MORF4L2 MRPL11 NKAP NUP62 PAWR PHF1 PID1 POLR2L POLR2M PPIG PRKAA1 PRR20A QKI RALYL RBM39 RIPPLY1 RP9P RPS25 SAP30BP SERF2 SLU7 STRBP TCEA2 TPM3 TRAF5 TRIM26 TTLL10 TXN2 U2AF2 WDYHV1 YES1 ZCCHC10 ZNF385C ZNF408 | |
Entrez ID | 9513 | 55145 | |
HPRD ID | 05629 | 15496 | |
Ensembl ID | ENSG00000129245 | ENSG00000131931 | |
Uniprot IDs | P51116 | Q9NVV9 | |
PDB IDs | 3H8Z | 2JTG 2KO0 2L1G | |
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | 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
|
assembled
childhood
compatible
confirms
contiguous
definite
deletions
distinctive
dystonia
dyt1
eighty
gch1
imprinted
ireland
laxity
maternally
microcephaly
myoclonus
nineteen
nkx2
phenotypically
probable
probands
progressing
sequenced
sgce
stature
uk
upper
|
|
Tagcloud (Difference) ? | 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
|
assembled
childhood
compatible
confirms
contiguous
definite
deletions
distinctive
dystonia
dyt1
eighty
gch1
imprinted
ireland
laxity
maternally
microcephaly
myoclonus
nineteen
nkx2
phenotypically
probable
probands
progressing
sequenced
sgce
stature
uk
upper
|
|
Tagcloud (Intersection) ? |