STXBP1 |
APBA2 |
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Gene Name | syntaxin binding protein 1 | amyloid beta (A4) precursor protein-binding, family A, member 2 | |
Image | No pdb structure | No pdb structure | |
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process |
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Pathways | |||
Drugs | |||
Diseases | |||
GWAS |
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Protein-Protein Interactions | 27 interactors: APBA1 APBA2 APP CDK5 CDK5R1 DOC2A DOC2B DYT10 HGS MAPT NEFH NEFM PLD1 PLD2 PRKCA PRKCB PRKCG SQSTM1 STX11 STX19 STX1A STX1B STX2 STX3 SYTL4 TRIM38 USO1 | 11 interactors: APP CLSTN1 CLSTN3 LRP1 LRP2 LRP8 MAPK6 NECAB3 NRXN1 RELA STXBP1 | |
Entrez ID | 6812 | 321 | |
HPRD ID | 04235 | 04090 | |
Ensembl ID | ENSG00000136854 | ENSG00000034053 | |
Uniprot IDs | B7Z1V5 P61764 Q68CM6 | Q59G28 Q99767 | |
PDB IDs | |||
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | 16p12
2q24
5q14
9q34
aetiology
caln1
cdkl5
cgh
cnv
cnvs
counselling
ehmt1
encephalopathies
encompassing
epileptic
etiological
grin2a
hypsarrhythmia
infantile
intronic
iss
kcnq2
magi2
mef2c
microdeletions
microduplications
scn2a
spasms
xq28
|
a4
ageing
apoe4
apolipoprotein
broadly
carrier
carriers
deposition
determinants
encode
endocytosis
epsilon4
fyn
implicate
influenced
initially
load
mediators
modify
modulators
physiology
pursue
referred
resembled
rnf219
sv2a
transcriptome
transcriptomic
unaffected
|
|
Tagcloud (Difference) ? | 16p12
2q24
5q14
9q34
aetiology
caln1
cdkl5
cgh
cnv
cnvs
counselling
ehmt1
encephalopathies
encompassing
epileptic
etiological
grin2a
hypsarrhythmia
infantile
intronic
iss
kcnq2
magi2
mef2c
microdeletions
microduplications
scn2a
spasms
xq28
|
a4
ageing
apoe4
apolipoprotein
broadly
carrier
carriers
deposition
determinants
encode
endocytosis
epsilon4
fyn
implicate
influenced
initially
load
mediators
modify
modulators
physiology
pursue
referred
resembled
rnf219
sv2a
transcriptome
transcriptomic
unaffected
|
|
Tagcloud (Intersection) ? |