Gene Name |
glutamate receptor, ionotropic, N-methyl D-aspartate 2A |
glutamate receptor, ionotropic, N-methyl-D-aspartate 3B |
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 |
- Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) ( 23453885)
- Hepatitis B ( 22004137)
- Thiazide-induced adverse metabolic effects in hypertensive patients ( 23400010)
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- Alzheimer's disease (late onset) ( 23571587)
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Protein-Protein Interactions |
27 interactors:
ACTN1
AP1M1
AP4M1
ARHGAP32
CAMK2A
CAMK2B
CASK
CDK5
DLG1
DLG2
DLG3
DLG4
DLGAP1
FYN
GRIN1
GRIN3A
GRIN3B
IL16
INADL
NEDD4
PLCG1
PRKCA
PTK2B
PTPN4
RGS3
SPTAN1
SRC
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2 interactors:
DLG4
GRIN2A
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Entrez ID |
2903 |
116444 |
HPRD ID |
00698 |
09444 |
Ensembl ID |
ENSG00000183454
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ENSG00000116032
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Uniprot IDs |
B4DII7
F5GZ52
Q12879
Q547U9
Q59EW6
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O60391
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PDB IDs |
3NFL
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
6j
6jxm
atg
autosomes
backcross
codon
crosses
dispersed
egr
epsilon
espilon
exons
f1xc57bl
flanking
grinl
interspecific
mapping
nucleas
polyadenylation
primer
s1
spans
spl
spretus
termination
zeta
|
asd
autism
compensation
counteract
de
disability
excitatory
exploring
grin1
grin2a
grin2c
grin2d
hypofunction
imbalance
implicate
instrumental
intellectual
neurodevelopment
neurodevelopmental
neurotransmission
nmdars
novo
scz
sequenced
sporadic
truncating
|
Tagcloud (Difference) ? |
6j
6jxm
atg
autosomes
backcross
codon
crosses
dispersed
egr
epsilon
espilon
exons
f1xc57bl
flanking
grinl
interspecific
mapping
nucleas
polyadenylation
primer
s1
spans
spl
spretus
termination
zeta
|
asd
autism
compensation
counteract
de
disability
excitatory
exploring
grin1
hypofunction
imbalance
implicate
instrumental
intellectual
neurodevelopment
neurodevelopmental
neurotransmission
nmdars
novo
scz
sequenced
sporadic
truncating
|
Tagcloud (Intersection) ? |
grin2a
grin2c
grin2d
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