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SDC2 and ITGB4
Data Source:
BioGRID
(two hybrid)
SDC2
ITGB4
Description
syndecan 2
integrin subunit beta 4
Image
GO Annotations
Cellular Component
Endoplasmic Reticulum Lumen
Golgi Lumen
Plasma Membrane
Cell Surface
Integral Component Of Membrane
Lysosomal Lumen
Collagen-containing Extracellular Matrix
Basement Membrane
Nucleolus
Plasma Membrane
Focal Adhesion
Integrin Complex
Basal Plasma Membrane
Cell Surface
Cell Junction
Hemidesmosome
Cell Leading Edge
Nuclear Membrane
Receptor Complex
Extracellular Exosome
Molecular Function
Protein Binding
PDZ Domain Binding
Identical Protein Binding
G Protein-coupled Receptor Binding
Integrin Binding
Protein Binding
Insulin-like Growth Factor I Binding
Neuregulin Binding
Biological Process
Retinoid Metabolic Process
Glycosaminoglycan Biosynthetic Process
Glycosaminoglycan Catabolic Process
Biological_process
Cell Migration
Post-translational Protein Modification
Cellular Protein Metabolic Process
Ephrin Receptor Signaling Pathway
Dendrite Morphogenesis
Regulation Of Dendrite Morphogenesis
Leukocyte Migration
Autophagy
Cell Adhesion
Cell-matrix Adhesion
Integrin-mediated Signaling Pathway
Response To Wounding
Cell Migration
Extracellular Matrix Organization
Hemidesmosome Assembly
Peripheral Nervous System Myelin Formation
Cell Adhesion Mediated By Integrin
Nail Development
Skin Morphogenesis
Filopodium Assembly
Mesodermal Cell Differentiation
Cell Motility
Trophoblast Cell Migration
Pathways
A tetrasaccharide linker sequence is required for GAG synthesis
HS-GAG biosynthesis
HS-GAG biosynthesis
HS-GAG degradation
Cell surface interactions at the vascular wall
Syndecan interactions
Syndecan interactions
Defective B4GALT7 causes EDS, progeroid type
Defective B3GAT3 causes JDSSDHD
Defective EXT2 causes exostoses 2
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
EPHB-mediated forward signaling
Defective B3GALT6 causes EDSP2 and SEMDJL1
Post-translational protein phosphorylation
Retinoid metabolism and transport
Assembly of collagen fibrils and other multimeric structures
Laminin interactions
Syndecan interactions
Type I hemidesmosome assembly
Drugs
Sargramostim
R1295
Diseases
Epidermolysis bullosa, junctional, including: Epidermolysis bullosa, junctional, Herlitz type (JEB-H); Epidermolysis bullosa, junctional, non-Herlitz type (JEB-nH); Epidermolysis bullosa, junctional, with pyloric atresia (JEB-PA)
GWAS
Post-traumatic stress disorder (
26114229
)
Refractive error (
32231278
)
Interacting Genes
28 interacting genes:
ANOS1
ASPH
BAG6
CASK
CSF2
CYP2C18
EPHB2
EZR
FGF2
FN1
HGF
ITGB4
LAMA3
NF1
PF4
PPP3CC
PRKCA
PRKCB
PRKCG
REG3A
SDCBP
SERPINA1
SERPINC1
SPARC
TGFB1
TGFBR3
TNFSF13
TRAPPC4
59 interacting genes:
ADAMTSL4
ALOX12
APPBP2
ATXN1
CLCA1
CLCA2
COL17A1
CYSRT1
DST
ECM1
EIF6
ERBB2
ERBIN
FYN
GRB2
HOXA1
ITGA6
KPRP
KRT31
KRT40
KRTAP1-1
KRTAP1-3
KRTAP10-7
KRTAP10-8
KRTAP10-9
KRTAP12-3
KRTAP15-1
KRTAP17-1
KRTAP2-3
KRTAP2-4
KRTAP3-1
KRTAP4-2
KRTAP6-2
KRTAP6-3
KRTAP9-2
KRTAP9-3
MDFI
MET
MID2
MTUS2
MYF5
NBPF19
NOTCH2NLA
PLEC
PLSCR4
POU2AF1
PRKCA
PRKCD
PTK2
SDC2
SDC3
SHC1
SREBF2
TGM1
TRIP6
VIM
YES1
YWHAB
YWHAQ
Entrez ID
6383
3691
HPRD ID
00803
00946
Ensembl ID
ENSG00000169439
ENSG00000132470
Uniprot IDs
A0A024R9D1
E9PBI9
P34741
A0A024R8K7
A0A024R8N2
A0A024R8T0
B7ZLD8
P16144
PDB IDs
6ITH
1QG3
2YRZ
3F7P
3F7Q
3F7R
3FQ4
3FSO
3H6A
4Q58
4WTW
4WTX
6GVK
6GVL
Enriched GO Terms of Interacting Partners
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Tagcloud (Difference)
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Tagcloud (Intersection)
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