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CD79A and STX3
Data Source:
BioGRID
(two hybrid)
CD79A
STX3
Description
CD79a molecule
syntaxin 3
Image
No pdb structure
GO Annotations
Cellular Component
Multivesicular Body
Plasma Membrane
External Side Of Plasma Membrane
Integral Component Of Membrane
B Cell Receptor Complex
Membrane Raft
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
Molecular Function
Transmembrane Signaling Receptor Activity
Protein Binding
Identical Protein Binding
SNARE Binding
SNAP Receptor Activity
Protein Binding
Arachidonic Acid Binding
Biological Process
Adaptive Immune Response
B Cell Differentiation
B Cell Proliferation
B Cell Activation
B Cell Receptor Signaling Pathway
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
Pathways
CD22 mediated BCR regulation
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers
Other interleukin signaling
Drugs
Diseases
Agammaglobulinemias, including the following six diseases: X-linked agammaglobulinemia (Bruton's agammaglobulinemia, XLA); IgM heavy chain gene deletions; Ig-alpha defect; Autosomal recessive agammaglobulinaemia; B cell-linker protein (BLNK) deficiency; Leucine-rich repeat-containing 8
GWAS
Brain morphology (MOSTest) (
32665545
)
High chromosomal aberration frequency (chromosome type) (
31586183
)
Interacting Genes
181 interacting genes:
ADIPOQ
AGTRAP
ALG10
ALG10B
ALG3
APOD
AQP1
AQP3
ATP6V0C
BCL2L2
BET1
BLK
BLNK
BRICD5
BTN2A2
C14orf180
C1GALT1
C2CD2L
C4orf3
CCDC167
CD19
CD5
CD79B
CDIPT
CLDN1
CLN6
CMTM5
CMTM7
CNIH1
CNIH3
COL4A5
CTSA
CTXN3
CYB561
CYB561A3
CYB561D2
CYB5B
DEFB127
DOLK
EDDM3B
EMC6
EMP1
EMP3
FA2H
FAM241B
FANCA
FATE1
FAXDC2
FCAR
FDFT1
FFAR3
FKBP8
FUNDC2
FXYD3
FYN
GALNT15
GIMAP1
GJB1
GPR42
HACD4
HCLS1
HMOX1
HMOX2
IER3
IGHM
INSIG2
ITGAM
JAGN1
JCHAIN
LAMB1
LCK
LEPROTL1
LHFPL5
LPAR3
LTC4S
LYN
MALL
MARCHF2
MFF
MFSD12
MFSD5
MFSD6
MGLL
MMD2
MOSPD3
MS4A13
MYADM
MYADML2
NAT8
NEU1
NINJ2
NIPAL3
NKG7
ORMDL2
OTOP2
PGAP2
PIGR
PKMYT1
PLP2
PLPP6
PLPPR2
PNLIPRP1
PRAF2
PTCH1
PTPN6
REEP6
RHO
RTP2
SACM1L
SEC22B
SERP1
SFTPC
SLC13A4
SLC13A5
SLC16A12
SLC16A13
SLC30A2
SLC35B1
SLC35B4
SLC38A1
SLC39A2
SLC39A9
SLC41A1
SLC41A2
SLC46A3
SLC66A2
SLC6A12
SLC7A1
SMCO4
SMIM3
STRIT1
STX12
STX3
STX8
SYK
SYNJ2BP
TECR
THBD
TM4SF19
TM4SF4
TMBIM6
TMEM107
TMEM11
TMEM128
TMEM140
TMEM147
TMEM14B
TMEM176A
TMEM187
TMEM19
TMEM218
TMEM222
TMEM229B
TMEM239
TMEM243
TMEM254
TMEM262
TMEM42
TMEM86A
TMEM86B
TMPPE
TNFRSF10C
TRAM1L1
TRARG1
TSNARE1
TSPAN2
TSPO2
UBE2J1
UBIAD1
UNC93B1
VAMP3
VAPA
VAPB
VTI1B
WFDC2
WFS1
YIF1A
YIPF4
YIPF6
ZDHHC15
ZDHHC22
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
Entrez ID
973
6809
HPRD ID
00203
15985
Ensembl ID
ENSG00000105369
ENSG00000166900
Uniprot IDs
P11912
Q13277
Q53YE2
PDB IDs
1CV9
Enriched GO Terms of Interacting Partners
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