Gene Name |
fragile X mental retardation, autosomal homolog 2 |
N-terminal EF-hand calcium binding protein 2 |
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 |
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
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53 interactors:
AIMP2
BEX2
BYSL
C1orf109
CAPN3
CARD9
CCDC146
CCDC151
CCDC153
CCDC33
CCNK
CENPO
DAXX
DFFA
DGCR6
DGCR6L
EHHADH
EIF4E2
FAM161A
FXR2
GCC1
GTPBP10
HAUS1
INPP1
ISCU
KANSL1
KDM1A
KIFC3
KLC3
KLC4
KPNA2
LENG1
LNX1
MED14
MRPS27
NEK6
NGFRAP1
NIP7
NOC4L
PRKAA2
PSMA1
RCOR3
RIC8A
RUNX1T1
SDCBP
SH2D4A
SSC5D
TEX11
TTC25
TTR
USP7
VTA1
WDYHV1
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Entrez ID |
9513 |
54550 |
HPRD ID |
05629 |
13263 |
Ensembl ID |
ENSG00000129245
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ENSG00000103154
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Uniprot IDs |
P51116
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Q7Z6G3
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PDB IDs |
3H8Z
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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
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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
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Tagcloud (Intersection) ? |
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