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STX3 and ZDHHC15
Data Source:
BioGRID
(two hybrid)
STX3
ZDHHC15
Description
syntaxin 3
zinc finger DHHC-type palmitoyltransferase 15
Image
No pdb structure
No pdb structure
GO Annotations
Cellular Component
Vacuole
Plasma Membrane
Cell-cell Junction
Synaptic Vesicle
Endomembrane System
Integral Component Of Membrane
Apical Plasma Membrane
Lamellipodium
Dendrite
Growth Cone
SNARE Complex
Melanosome
Specific Granule
Azurophil Granule
Zymogen Granule Membrane
Neuron Projection
Presynaptic Active Zone Membrane
Extracellular Exosome
Schaffer Collateral - CA1 Synapse
Postsynapse
Glutamatergic Synapse
Golgi Membrane
Endoplasmic Reticulum
Golgi Apparatus
Postsynaptic Density
Integral Component Of Golgi Membrane
Postsynapse
Molecular Function
SNARE Binding
SNAP Receptor Activity
Protein Binding
Arachidonic Acid Binding
Protein Binding
Zinc Ion Binding
Palmitoyltransferase Activity
Protein-cysteine S-palmitoyltransferase Activity
Biological Process
Intracellular Protein Transport
Exocytosis
Vesicle Fusion
Positive Regulation Of Cell Population Proliferation
Synaptic Vesicle Docking
Cytokine-mediated Signaling Pathway
Neuron Projection Development
Synaptic Vesicle Fusion To Presynaptic Active Zone Membrane
Positive Regulation Of Cell Adhesion
Vesicle Docking
Positive Regulation Of Chemotaxis
Long-term Synaptic Potentiation
Exocytic Insertion Of Neurotransmitter Receptor To Postsynaptic Membrane
Positive Regulation Of Protein Localization To Plasma Membrane
Positive Regulation Of Protein Localization To Cell Surface
Protein Targeting To Membrane
Synaptic Vesicle Maturation
Protein Phosphopantetheinylation
Peptidyl-L-cysteine S-palmitoylation
Protein Palmitoylation
Regulation Of Dendritic Spine Morphogenesis
Protein Localization To Postsynapse
Protein Localization To Membrane
Protein Targeting To Golgi Apparatus
Positive Regulation Of Dendrite Development
Pathways
Other interleukin signaling
Drugs
Diseases
Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
GWAS
High chromosomal aberration frequency (chromosome type) (
31586183
)
Interacting Genes
52 interacting genes:
AQP6
CD79A
COQ9
CPLX2
CPLX4
CREB3L1
CYB561
DNAJC5
EBAG9
ELOVL4
ERGIC3
EVI5
FAM209A
FXYD3
GPR152
GPX8
JAGN1
LMNA
MANBAL
MFSD14B
MGST3
MMGT1
MSMO1
MTIF3
NAPB
PGRMC2
REEP4
RMDN3
SCN3B
SLC35C2
SNAP23
SNAP25
SNAP29
STX1A
STX2
STX4
STX5
STXBP1
STXBP2
SYT1
SYT4
SYT7
TBC1D30
TMEM14B
TMPPE
TMX2
TRPC3
TXLNA
VAMP3
VAMP7
VAMP8
ZDHHC15
48 interacting genes:
ADCYAP1R1
ARL13B
BNIP3
C14orf180
CD79A
CELA2B
CERCAM
CLEC10A
CLRN1
CREB3L1
CYB5R3
DHRSX
ERGIC3
FAM241B
GIMAP1
GOLGA7B
GPR152
LEMD1
LEPROTL1
LHFPL5
LMNA
LSMEM1
MCEMP1
MTIF3
ORMDL1
ORMDL2
PEX16
PLLP
PRAF2
PVR
RUSF1
SLC10A6
SMIM1
SNORC
STX3
TBXA2R
TMEFF2
TMEM120B
TMEM128
TMEM14C
TMEM222
TMEM42
TMEM52B
TNFRSF10B
TSNARE1
TUFM
VAPB
YIPF4
Entrez ID
6809
158866
HPRD ID
15985
06758
Ensembl ID
ENSG00000166900
ENSG00000102383
Uniprot IDs
Q13277
Q53YE2
B3KY34
Q96MV8
PDB IDs
Enriched GO Terms of Interacting Partners
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Tagcloud
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Tagcloud (Difference)
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Tagcloud (Intersection)
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