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LNPK and SYP
Data Source:
BioGRID
(two hybrid)
LNPK
SYP
Description
lunapark, ER junction formation factor
synaptophysin
Image
No pdb structure
No pdb structure
GO Annotations
Cellular Component
Nucleoplasm
Endoplasmic Reticulum
Endoplasmic Reticulum Membrane
Integral Component Of Membrane
Integral Component Of Endoplasmic Reticulum Membrane
Endoplasmic Reticulum Tubular Network
Endoplasmic Reticulum Tubular Network Membrane
Synaptic Vesicle
Integral Component Of Synaptic Vesicle Membrane
Synaptic Vesicle Membrane
Neuromuscular Junction
Presynaptic Membrane
Neuron Projection
Terminal Bouton
Perinuclear Region Of Cytoplasm
Presynaptic Active Zone
Excitatory Synapse
Schaffer Collateral - CA1 Synapse
Molecular Function
Identical Protein Binding
Metal Ion Binding
Protein Binding
Cholesterol Binding
Syntaxin-1 Binding
SH2 Domain Binding
Identical Protein Binding
Protein Self-association
Biological Process
Endoplasmic Reticulum Organization
Blood Coagulation
Regulation Of Chondrocyte Differentiation
Embryonic Forelimb Morphogenesis
Embryonic Digit Morphogenesis
Limb Development
Endoplasmic Reticulum Tubular Network Organization
Endoplasmic Reticulum Tubular Network Maintenance
Positive Regulation Of Endoplasmic Reticulum Tubular Network Organization
Endocytosis
Synaptic Vesicle Maturation
Regulation Of Neuronal Synaptic Plasticity
Regulation Of Long-term Neuronal Synaptic Plasticity
Regulation Of Short-term Neuronal Synaptic Plasticity
Synaptic Vesicle Endocytosis
Synaptic Vesicle Membrane Organization
Cellular Response To Organic Substance
Regulation Of Synaptic Vesicle Exocytosis
Regulation Of Opioid Receptor Signaling Pathway
Pathways
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
Interacting Genes
12 interacting genes:
ANXA1
CAND1
CHMP1A
KLHL12
LMO3
NOC4L
PAX6
PLIN3
SYP
UBC
UBE2D1
YIF1A
41 interacting genes:
AP1G1
ARFIP2
CAND2
CD160
DIABLO
FARS2
GAB1
GDNF
GRB2
HSFX1
HSFX2
JOSD2
LNPK
MIEF1
MIEF2
MRM1
MRRF
MTERF3
MYG1
NDRG4
PBX3
PITPNC1
PLIN3
PNKP
PPIF
PTCD1
PTPN9
RBFA
SH3GLB1
SIAH1
SIAH2
SMG9
SNX1
SPG21
SSX5
STARD4
THAP4
TUFM
VAMP2
WDFY2
WIPI2
Entrez ID
80856
6855
HPRD ID
13886
02435
Ensembl ID
ENSG00000144320
ENSG00000102003
Uniprot IDs
B7Z829
Q9C0E8
P08247
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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