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HSPG2 and CACNA1A
Data Source:
BioGRID
(two hybrid)
HSPG2
CACNA1A
Description
heparan sulfate proteoglycan 2
calcium voltage-gated channel subunit alpha1 A
Image
GO Annotations
Cellular Component
Extracellular Region
Basement Membrane
Extracellular Space
Golgi Lumen
Plasma Membrane
Focal Adhesion
Lysosomal Lumen
Collagen-containing Extracellular Matrix
Extracellular Exosome
Plasma Membrane Protein Complex
Nucleus
Cytoplasm
Plasma Membrane
Voltage-gated Calcium Channel Complex
Integral Component Of Membrane
Cell Projection
Neuronal Cell Body
Synapse
Molecular Function
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
Amyloid-beta Binding
Voltage-gated Calcium Channel Activity
Protein Binding
High Voltage-gated Calcium Channel Activity
Syntaxin Binding
Metal Ion Binding
Biological Process
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
Calcium Ion Transport
Positive Regulation Of Cytosolic Calcium Ion Concentration
Chemical Synaptic Transmission
Cell Death
Regulation Of Ion Transmembrane Transport
Regulation Of Insulin Secretion
Modulation Of Chemical Synaptic Transmission
Membrane Depolarization
Calcium Ion Import
Calcium Ion Transmembrane Transport
Response To Amyloid-beta
Cellular Response To Amyloid-beta
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
Presynaptic depolarization and calcium channel opening
Regulation of insulin secretion
Drugs
Palifermin
Ergocalciferol
Enflurane
Phenytoin
Spironolactone
Magnesium sulfate
Verapamil
Levomenthol
Loperamide
Bepridil
Ziconotide
Dotarizine
Trimebutine
Benidipine
Cilnidipine
Lacidipine
Manidipine
Butamben
Bioallethrin
Bioallethrin
Bioallethrin
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
Episodic ataxias
Familial or sporadic hemiplegic migraine
Spinocerebellar ataxia (SCA); Machado-Joseph disease (SCA3)
GWAS
Atrial fibrillation (
30061737
)
Height (
28552196
)
PR interval (
32439900
)
Exfoliation syndrome (
25706626
)
Proteinuria and chronic kidney disease (
26420894
)
Interacting Genes
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
92 interacting genes:
ABCA2
ABI1
ACTN1
ADGRL1
AGRN
ALDOA
AMIGO2
AP2M1
ARHGAP22
BTG3
C1QTNF1
CABP1
CACNB1
CACNB4
CALM2
CALM3
CKAP5
CRIM1
CRMP1
CSNK2B
CYSRT1
DNAJB5
EFEMP1
EFEMP2
EHMT2
EIF3A
FBLN1
GET3
GNB1
GOLGA6L5P
GRN
HECW1
HHATL
HIVEP1
HSPG2
IP6K1
JAG2
KALRN
KHDRBS3
KIAA1191
LAMB1
LLGL1
LRP1
LTBP1
LTBP3
LTBP4
MANBAL
MATK
MATN2
MEGF6
MEGF8
MIA3
MOAP1
NDUFB8
NELFCD
NELL1
NELL2
NOTCH1
NOXA1
OLIG1
PCSK5
PCSK6
PMM1
PPIG
PPM1A
PPP1R12C
PTGDS
PUF60
RBM12B
RIMBP2
RPL31
RPS17
SCP2
SPRY1
SRRM4
SRSF1
SUMF2
SYT1
TAF15
TELO2
TSC22D1
TSPAN7
TSPOAP1
TUBB2B
UQCRC2
VARS1
VPS52
VWF
WBP1
YLPM1
ZCCHC17
ZNF233
Entrez ID
3339
773
HPRD ID
00804
03004
Ensembl ID
ENSG00000142798
ENSG00000141837
Uniprot IDs
P98160
A0A087WW63
B5TYJ1
O00555
Q9NS89
PDB IDs
3SH4
3SH5
3BXK
Enriched GO Terms of Interacting Partners
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