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MTDH and HSPG2
Data Source:
BioGRID
(unspecified method)
MTDH
HSPG2
Description
metadherin
heparan sulfate proteoglycan 2
Image
GO Annotations
Cellular Component
Fibrillar Center
Nucleus
Cytoplasm
Endoplasmic Reticulum
Endoplasmic Reticulum Membrane
Bicellular Tight Junction
Integral Component Of Membrane
Apical Plasma Membrane
Nuclear Body
Nuclear Membrane
Intercellular Canaliculus
Perinuclear Region Of Cytoplasm
Extracellular Region
Basement Membrane
Extracellular Space
Golgi Lumen
Plasma Membrane
Focal Adhesion
Lysosomal Lumen
Collagen-containing Extracellular Matrix
Extracellular Exosome
Plasma Membrane Protein Complex
Molecular Function
RNA Polymerase II Transcription Factor Binding
Transcription Coregulator Activity
Transcription Coactivator Activity
RNA Binding
Double-stranded RNA Binding
Protein Binding
NF-kappaB Binding
Amyloid-beta Binding
Calcium Ion Binding
Protein Binding
Protein C-terminus Binding
Extracellular Matrix Structural Constituent Conferring Compression Resistance
Low-density Lipoprotein Particle Receptor Binding
Biological Process
Negative Regulation Of Transcription By RNA Polymerase II
Regulation Of Transcription By RNA Polymerase II
Positive Regulation Of Autophagy
Lipopolysaccharide-mediated Signaling Pathway
Negative Regulation Of Apoptotic Process
Positive Regulation Of I-kappaB Kinase/NF-kappaB Signaling
Positive Regulation Of Angiogenesis
Positive Regulation Of Transcription, DNA-templated
Positive Regulation Of NF-kappaB Transcription Factor Activity
Positive Regulation Of Protein Kinase B Signaling
Bicellular Tight Junction Assembly
Retinoid Metabolic Process
Angiogenesis
Glycosaminoglycan Biosynthetic Process
Glycosaminoglycan Catabolic Process
Lipid Metabolic Process
Receptor-mediated Endocytosis
Inflammatory Response
Brain Development
Animal Organ Morphogenesis
Tissue Development
Negative Regulation Of Angiogenesis
Cell Differentiation
Extracellular Matrix Organization
Cellular Protein Metabolic Process
Circulatory System Development
Pathways
Degradation of the extracellular matrix
Degradation of the extracellular matrix
A tetrasaccharide linker sequence is required for GAG synthesis
HS-GAG biosynthesis
HS-GAG biosynthesis
HS-GAG degradation
Integrin cell surface interactions
Laminin interactions
Laminin interactions
Non-integrin membrane-ECM interactions
Non-integrin membrane-ECM interactions
ECM proteoglycans
Defective B4GALT7 causes EDS, progeroid type
Defective B3GAT3 causes JDSSDHD
Defective EXT2 causes exostoses 2
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
Defective B3GALT6 causes EDSP2 and SEMDJL1
Retinoid metabolism and transport
Amyloid fiber formation
Drugs
Palifermin
Diseases
Heparan sulfate proteoglycan gene defects, including: Dyssegmental dysplasia, Silverman-Handmaker type; Schwartz-Jampel syndrome; Simpson-Golabi-Behmel syndrome, type 1; Omodysplasia 1; Multiple exostoses
GWAS
Mean corpuscular hemoglobin (
29403010
32888494
)
Mean corpuscular hemoglobin concentration (
32888494
)
Mean corpuscular volume (
32888494
)
Migraine (
20802479
)
Nicotine metabolite ratio in current smokers (
27488534
)
Plasma parathyroid hormone levels (
30134803
)
Red cell distribution width (
32888494
27863252
28957414
)
Sweet taste preference (
32572145
)
Atrial fibrillation (
30061737
)
Height (
28552196
)
PR interval (
32439900
)
Interacting Genes
175 interacting genes:
ABCA12
ABCC3
ABTB1
ACTN1
ADCK2
ADGRA2
AGAP3
ALOX5
ANKRD13D
ANKRD26P1
ANPEP
ARNT2
ARRDC1
AXL
BCAS3
BCS1L
CAPN2
CARD8
CCL20
CCN2
CCNDBP1
CCT4
CD109
CD22
CDC14B
CDC42
CENPJ
CEP162
CLCN7
CLDN2
CLMN
COL13A1
COL4A4
COL6A1
CPT2
CRIM1
CSNK2A1
CTSB
CUL7
CUL9
CYFIP2
CYP27A1
CYP4V2
DMTF1
DNAH5
DNAI4
DOCK2
DOP1B
DSP
DUSP5
ECE1
EGFR
EGR1
ELN
EML1
EPHB1
EPHX2
ERCC2
ERICH6B
ESAM
FAM184A
FANCI
FASN
FCGRT
FLNA
FLNC
FN1
GHDC
GLG1
GRID1
HACE1
HERC5
HP1BP3
HSPG2
ICA1L
IFT46
IKBKB
IL17RA
IL2RB
IPO9
IRS2
ITGB5
ITPR3
JADE3
JAG1
KCNH1
KCNQ5
KDM6A
KMT2B
LAMA5
LDLRAD2
LOXL4
LRIG3
LRP1
LRP5
MAP3K12
MCM6
MEGF11
METTL3
MLPH
MMP2
MNT
MRC2
MRPL39
MYH9
MYL5
NEB
NEO1
NFKB2
NOTCH3
NPC1
NPR1
NUP210
NXF4
OBSCN
OGT
OR8G5
OSMR
PCCB
PCDH7
PDCD11
PKN1
PLAT
PLD2
PLEC
PLEKHO2
PLXNA3
PPFIA2
PRICKLE4
PSIP1
PTHLH
PWP2
RAB24
RGS13
RIN1
RIPK1
RNF123
RNF213
RSPO3
RYR1
SDK1
SELENOI
SEZ6L2
SGSM2
SH2B2
SIAE
SLC22A18AS
SLC38A4
SPEF2
SPRED2
SPTBN5
SQSTM1
SSH3
STEAP3
STK25
STXBP1
SYNE1
TACR2
TBC1D2B
TBCD
TCIRG1
TEP1
THBS1
THSD4
TINAGL1
TNS2
TOPORS
TRAPPC12
TRPC4AP
TUBB3
VIM
WDFY2
WNK2
ZNF559
ZXDC
32 interacting genes:
APP
ATF7IP
ATN1
BMP1
CACNA1A
CCN2
COL13A1
ECM1
FBLN1
FBLN2
FBN1
FGF2
FGF7
FGFBP1
FN1
GFI1B
GRN
ITGA2
ITGB1
LAMA1
MTDH
NID1
NID2
PDGFA
PDGFB
PRELP
PRPF40A
SPARC
TCAP
TTR
UBC
VWA1
Entrez ID
92140
3339
HPRD ID
17459
00804
Ensembl ID
ENSG00000147649
ENSG00000142798
Uniprot IDs
A0A024R9D2
Q86UE4
P98160
PDB IDs
4QMG
3SH4
3SH5
Enriched GO Terms of Interacting Partners
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