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ANXA7 and ACTB
Data Source:
BioGRID
(two hybrid)
ANXA7
ACTB
Description
annexin A7
actin beta
Image
No pdb structure
GO Annotations
Cellular Component
Nucleus
Cytoplasm
Endoplasmic Reticulum Membrane
Membrane
Chromaffin Granule Membrane
Collagen-containing Extracellular Matrix
Extracellular Exosome
Chromatin
Extracellular Space
Nucleus
Nucleoplasm
Cytoplasm
Cytosol
Cytoskeleton
Actin Filament
Plasma Membrane
Cell-cell Junction
Adherens Junction
Focal Adhesion
Actin Cytoskeleton
Membrane
Lamellipodium
Axon
Vesicle
Protein-containing Complex
NuA4 Histone Acetyltransferase Complex
Cytoplasmic Ribonucleoprotein Granule
Apical Junction Complex
Synapse
Extracellular Exosome
Tight Junction
Blood Microparticle
Dense Body
Presynapse
Postsynaptic Actin Cytoskeleton
Glutamatergic Synapse
Ribonucleoprotein Complex
Molecular Function
RNA Binding
Integrin Binding
Calcium Ion Binding
Protein Binding
Calcium-dependent Phospholipid Binding
Calcium-dependent Protein Binding
Structural Constituent Of Cytoskeleton
Protein Binding
ATP Binding
Kinesin Binding
Protein Kinase Binding
Tat Protein Binding
Nucleosomal DNA Binding
Identical Protein Binding
Tau Protein Binding
Nitric-oxide Synthase Binding
Structural Constituent Of Postsynaptic Actin Cytoskeleton
Biological Process
Autophagy
Negative Regulation Of Gene Expression
Response To Organic Cyclic Compound
Epithelial Cell Differentiation
Response To Calcium Ion
Membrane Fusion
Regulation Of Cyclin-dependent Protein Serine/threonine Kinase Activity
Morphogenesis Of A Polarized Epithelium
Retina Homeostasis
Establishment Or Maintenance Of Cell Polarity
Axonogenesis
Protein Deubiquitination
Substantia Nigra Development
Regulation Of Transmembrane Transporter Activity
Negative Regulation Of Protein Binding
Cell Junction Assembly
Adherens Junction Assembly
Maintenance Of Blood-brain Barrier
Fc-gamma Receptor Signaling Pathway Involved In Phagocytosis
ATP-dependent Chromatin Remodeling
Apical Protein Localization
Positive Regulation Of Gene Expression, Epigenetic
Ephrin Receptor Signaling Pathway
Cell Motility
Regulation Of Norepinephrine Uptake
Positive Regulation Of Norepinephrine Uptake
Membrane Organization
Platelet Aggregation
Protein Localization To Adherens Junction
Cellular Response To Cytochalasin B
Postsynaptic Actin Cytoskeleton Organization
Regulation Of Transepithelial Transport
Regulation Of Protein Localization To Plasma Membrane
Pathways
Translocation of SLC2A4 (GLUT4) to the plasma membrane
Gap junction degradation
Formation of annular gap junctions
Regulation of actin dynamics for phagocytic cup formation
Regulation of actin dynamics for phagocytic cup formation
HATs acetylate histones
Prefoldin mediated transfer of substrate to CCT/TriC
Folding of actin by CCT/TriC
EPHB-mediated forward signaling
EPH-ephrin mediated repulsion of cells
Adherens junctions interactions
Adherens junctions interactions
Recycling pathway of L1
Recycling pathway of L1
VEGFA-VEGFR2 Pathway
Interaction between L1 and Ankyrins
Interaction between L1 and Ankyrins
Cell-extracellular matrix interactions
B-WICH complex positively regulates rRNA expression
RHO GTPases activate IQGAPs
RHO GTPases Activate WASPs and WAVEs
RHO GTPases Activate WASPs and WAVEs
RHO GTPases Activate Formins
RHO GTPases Activate Formins
MAP2K and MAPK activation
UCH proteinases
DNA Damage Recognition in GG-NER
Signaling by moderate kinase activity BRAF mutants
Signaling by high-kinase activity BRAF mutants
Signaling by BRAF and RAF fusions
Paradoxical activation of RAF signaling by kinase inactive BRAF
Clathrin-mediated endocytosis
Signaling downstream of RAS mutants
Signaling by RAF1 mutants
FCGR3A-mediated phagocytosis
FCGR3A-mediated phagocytosis
Factors involved in megakaryocyte development and platelet production
Drugs
Quercetin
Phenethyl Isothiocyanate
Diseases
Other phagocyte defects, including the following eight diseases: Chediak-Higashi syndrome; Griscelli syndrome, type 1 (GS1); Griscelli syndrome, type 2 (GS2); Griscelli syndrome, type 3 (GS3); beta-actin deficiency; Neutrophil-specific granule deficiency; Myeloperoxidase deficiency; Glucose 6-phosphate dehydrogenase deficiency; Shwachman syndrome
GWAS
Copper levels (
26025379
)
Global electrical heterogeneity phenotypes (
29622589
)
High light scatter reticulocyte percentage of red cells (
32888494
)
Lymphocyte counts (
32888494
)
Mean corpuscular hemoglobin (
32888494
)
Mean corpuscular hemoglobin concentration (
32888494
)
Monocyte count (
32888494
)
Relative hand skill in reading disability (
24068947
)
Reticulocyte count (
32888494
)
Reticulocyte fraction of red cells (
32888494
)
Triglyceride levels (
32203549
)
Interacting Genes
107 interacting genes:
A1BG
A2M
ACTB
ACTL6B
ADAMTS10
ANGPT2
APC
APLP1
ATP5F1B
ATP6V1A
ATXN3
BAG6
CCDC90B
CCT7
CDK4
CELF3
CENPB
CHGB
CLEC3B
COL11A2
COL4A2
COL4A5
COPS6
CPNE2
CPNE6
CRMP1
CSAD
CTSB
DDAH2
DMPK
DOCK7
DVL1
DYNC1I1
EEF1A1
ERG28
EXT2
F13A1
FAF1
FBN3
FGB
FLAD1
GAPDH
GBP2
GDF9
GNB2
GNB5
HADHB
HMGXB3
HOXD8
INPP5K
INTS11
KLHL23
KMT2B
LRIF1
MED31
MPPED1
MSH2
NGFR
NMT2
NPRL2
OTUB1
PAAF1
PAX8
PDCD6
PDHB
PKM
PLD3
PRKACA
PRKCA
PRKCB
PRKCG
PRKG1
PSMB10
QARS1
RBBP4
RBM48
RPA1
RPL13
RPS2
S100A10
SDF4
SEMA5B
SETDB1
SMPD1
SP110
SRC
SRI
SUMO3
TAF5L
TIAM2
TLE1
TMEM108
TMSB4X
TRMT2A
TUBA1A
TUBB2B
TUBB3
UBE2D1
UCHL5
UNC119
USP4
VIM
WDR18
WDR73
ZBTB16
ZNF135
ZNF431
157 interacting genes:
A2M
ABLIM1
ABRA
ACD
ACTC1
ACTG1
AIMP2
ALOX5
ANXA7
AQP2
AR
ARPC1B
ATF7IP
BBS4
BCL2L1
CAP1
CAPZA1
CCN2
CCT2
CCT4
CCT5
CCT8
CDC37
CDK5R2
CDKN1A
CDKN2A
CFL1
CFL2
CLIC4
CLNS1A
CNN2
CORO1A
CORO7
COTL1
CPNE1
CPNE2
CPNE4
CSNK1A1
CSNK2B
DMTN
DNASE1
DSTN
DUSP19
DYNLL1
EEF1A1
EHHADH
EMD
EP300
ERG
EZR
FABP4
FHL3
FLII
GAPDH
GNA12
GSN
H2AX
HCK
HIP1R
HMMR
HNRNPAB
HNRNPD
HNRNPU
HSD17B4
HSPB2
HTR6
KHDRBS1
LASP1
LGALS13
LINC01554
LINC02582
LMNA
LMOD1
LRRK2
LYN
MAP1B
MAP2
MAPT
MRGBP
MTNR1A
MX1
MYO18B
MYO1E
MYOC
NCALD
NCF1
NDEL1
NEBL
NOS2
NRAP
NSMAF
NT5E
NTAQ1
P2RX7
PCYT1A
PDIA2
PDLIM5
PFDN1
PFDN4
PFN1
PFN2
PHACTR4
PLD1
PLD2
PLG
POLR2A
POT1
PRKCD
PROSER2
PTN
PTPRF
RAB4A
RAC1
RAC2
RCC1
RNF4
RPL10A
S100A11
SAMHD1
SCN10A
SHBG
SMAD3
SMAD9
SMARCA4
SMN1
SPTAN1
SPTB
SPTBN2
SRPK2
SSH1
SSH2
SSH3
STX4
SUMO2
SYNJ2BP
TANC1
TGM2
TINF2
TK1
TMSB4X
TMSB4XP1
TMSB4XP4
TNNI2
TPM1
TPM2
TPM3
TRIM15
TSHR
TTR
UBE2I
UBE3A
VHL
VSNL1
WASF1
WASF2
WASF3
XPO6
Entrez ID
310
60
HPRD ID
01720
00032
Ensembl ID
ENSG00000138279
ENSG00000075624
Uniprot IDs
B2R657
P20073
P60709
Q1KLZ0
PDB IDs
3BYH
3D2U
3J82
3LUE
6ANU
6ICT
6ICV
6LTJ
6MBJ
6MBK
6MBL
6NBW
6OX0
6OX1
6OX2
6OX3
6OX4
6OX5
Enriched GO Terms of Interacting Partners
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Tagcloud (Intersection)
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