Gene Name |
fragile X mental retardation, autosomal homolog 2 |
RNA binding protein with multiple splicing |
Image |
|
|
Gene Ontology Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
|
- Heart rate variability traits ( 22174390)
|
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
|
174 interactors:
ADAM15
AES
AMMECR1
APLN
ARHGAP9
ARHGEF39
ARID5A
ATN1
ATP6V0E2
ATXN1
BANP
BBS2
BCL6B
BHLHE40
BOLL
C11orf87
C1orf111
C1orf94
C20orf195
C22orf39
C9orf24
CAMK2B
CCER1
CCNG1
CCNK
CDC23
CDC42EP1
CNNM3
CRBN
CREB5
CRYBA1
CSN3
CSNK1G2-AS1
CYBA
DAZAP2
DCAF8
DCDC2B
DCTN5
DMRT3
DOK3
DOK6
DPYSL4
DTX2
DVL2
EFEMP2
ENKD1
EWSR1
EYA2
FAM103A1
FAM124B
FAM168A
FASTK
FBF1
FBXL18
FOXC2
FOXP3
FOXS1
FXR2
GCM2
GLYCTK
GPATCH2L
GPS2
GRAP
GRAP2
GSE1
HEY2
HEYL
HNRNPLL
HOXA1
HOXA9
HOXB9
IGF2
ILF3
INCA1
INIP
IP6K2
KCTD9
KIF1A
KIR2DL4
KPNA2
KRAS
KRTAP12-2
KRTAP19-5
KRTAP19-7
KRTAP23-1
KRTAP8-1
LGALS9C
LINC00482
LINC00588
LINC00908
LINC01547
LINC01588
LMO4
LOC142937
LOC148413
LONRF1
LRRC41
LRRC75A-AS1
LZTS2
MAGED1
MCM5
MGAT5B
MVP
MYOZ2
NAB2
NAPRT
NEDD9
NEU4
NR1D2
NYNRIN
OTX1
PAPD4
PDLIM4
PER1
PGLS
PHF1
PIH1D1
PIN1
PITX1
PLAC8
POGZ
POM121
PRKAA1
PRKAA2
PRKAB2
PRR20A
QKI
R3HDM2
RABL6
RBFOX1
RBFOX2
RDH12
RHOBTB3
RHOXF2
RIPPLY1
ROR2
RTP5
RUSC1
SBF2
SEMA4G
SERF2
SF1
SH3RF2
SIRPB1
SMUG1
SNRPB
SNRPC
SPATA8
SPG7
STRBP
TBX6
TEX37
TFG
TIE1
TINAGL1
TMSB4X
TOLLIP
TOR1AIP2
TRIP13
TTLL10
TUSC2
VENTX
VHL
VHLL
VPS37C
WDR54
WDR90
WDYHV1
YPEL3
ZBTB32
ZC3H10
ZNF385C
ZNF488
ZNF581
|
Entrez ID |
9513 |
11030 |
HPRD ID |
05629 |
11870 |
Ensembl ID |
ENSG00000129245
|
ENSG00000157110
|
Uniprot IDs |
P51116
|
B4E3T4
D3DSV0
Q93062
|
PDB IDs |
3H8Z
|
1BNY
|
Enriched GO Terms of Interacting Partners? |
|
|
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
|
|
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
|
|
Tagcloud (Intersection) ? |
|