Gene Name |
glutamate receptor, ionotropic, N-methyl D-aspartate 1 |
heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A) |
Image |
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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 |
- Post-traumatic stress disorder (asjusted for relatedness) ( 23726511)
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Protein-Protein Interactions |
53 interactors:
ACTN2
AKAP9
CALM1
CAMK2A
CAMK2G
CANX
CDH2
CIT
CLTC
CTNNB1
DLG2
DLG3
DLG4
DLGAP4
DNM1
DRD1
DUSP4
EPHB2
EPHB4
FUS
FYN
GRIN2A
GRIN2B
GRIN2D
GRIN3A
HNRNPU
HRAS
HSPA1A
INA
LNX1
LRP8
MAP2
MAP2K2
MYH9
NANOS1
NEFL
NF1
PLAT
PLCG1
PPP2R1A
PPP2R2A
PRKCA
PRKCB
PRKCE
PRKCG
RAP2A
RPS6KA3
SP3
SPTAN1
SYNGAP1
TJP1
TRAF3
TUBA4B
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35 interactors:
ACTB
BTRC
CASP3
CD5
CDKN2A
CR2
ELL
EP300
ERG
GAS7
GRIN1
GRIN2D
GTF2H1
HNRNPD
HNRNPH3
IL7R
KAT2B
NDN
NDRG1
NEDD4
NR3C1
PIN1
POLR2A
POU3F4
PRMT1
PRPF40A
PTPN11
SMN1
SREK1
STAU1
SYK
TCERG1
WBP4
YAP1
ZNF689
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Entrez ID |
2902 |
3192 |
HPRD ID |
15926 |
04185 |
Ensembl ID |
ENSG00000176884
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ENSG00000153187
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Uniprot IDs |
Q05586
Q59GW0
Q5VSF9
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Q00839
Q96BA7
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PDB IDs |
2HQW
2NR1
3BYA
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1ZRJ
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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17p13
1q21
1q44
2q23
2q31
agilent
annotations
asd
autism
backgrounds
cgh
cnv
cnvs
disabilities
dissect
encephalopathy
epileptic
exome
expand
hallux
implicates
infantile
intellectual
lissencephaly
mbd5
microcephaly
pafah1b1
pathogenicity
spasms
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Tagcloud (Difference) ? |
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17p13
1q21
1q44
2q23
2q31
agilent
annotations
asd
autism
backgrounds
cgh
cnv
cnvs
disabilities
dissect
encephalopathy
epileptic
exome
expand
hallux
implicates
infantile
intellectual
lissencephaly
mbd5
microcephaly
pafah1b1
pathogenicity
spasms
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Tagcloud (Intersection) ? |
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