SCEL |
FXR2 |
||
---|---|---|---|
Gene Name | sciellin | 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 | 8 interactors: APP FXR2 GOLGA2 KIFC3 MTUS2 NMI TSGA10 TXNIP | 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 | 8796 | 9513 | |
HPRD ID | 09161 | 05629 | |
Ensembl ID | ENSG00000136155 | ENSG00000129245 | |
Uniprot IDs | O95171 | P51116 | |
PDB IDs | 3H8Z | ||
Enriched GO Terms of Interacting Partners? |
|
|
|
Tagcloud ? | accordance
advanced
already
appeared
attach
authors
behavior
ceruloplasmin
copper
diagnostic
digestive
evolution
gastroenteric
gastrointestinal
inclined
intestine
large
neoplasms
observations
particular
polychemotherapy
relation
remission
scl
seem
stomach
tendency
untreated
variation
|
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) ? | accordance
advanced
already
appeared
attach
authors
behavior
ceruloplasmin
copper
diagnostic
digestive
evolution
gastroenteric
gastrointestinal
inclined
intestine
large
neoplasms
observations
particular
polychemotherapy
relation
remission
scl
seem
stomach
tendency
untreated
variation
|
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) ? |