NCAN and CNTN2

Number of citations of the paper that reports this interaction (PubMedID 8663515)
35

Data Source:
BioGRID (pull down)
HPRD (in vitro)

		NCAN	CNTN2
Description		neurocan	contactin 2
Image		No pdb structure
GO Annotations	Cellular Component	Extracellular Region Golgi Lumen Extracellular Matrix Lysosomal Lumen	Plasma Membrane Cell Surface Axon Node Of Ranvier Neuronal Cell Body Myelin Sheath Juxtaparanode Region Of Axon Synapse Anchored Component Of Postsynaptic Membrane
	Molecular Function	Calcium Ion Binding Hyaluronic Acid Binding Carbohydrate Binding	Carbohydrate Binding Identical Protein Binding Protein Self-association Cell-cell Adhesion Mediator Activity
	Biological Process	Skeletal System Development Cell Adhesion Central Nervous System Development Extracellular Matrix Organization Chondroitin Sulfate Biosynthetic Process Chondroitin Sulfate Catabolic Process Dermatan Sulfate Biosynthetic Process	Microtubule Cytoskeleton Organization Cell Adhesion Homophilic Cell Adhesion Via Plasma Membrane Adhesion Molecules Axon Guidance Axonal Fasciculation Learning Adult Walking Behavior Positive Regulation Of Protein Processing Cerebral Cortex GABAergic Interneuron Migration Central Nervous System Myelination Regulation Of Axon Diameter Receptor Internalization Clustering Of Voltage-gated Potassium Channels Negative Regulation Of Neuron Differentiation Regulation Of Neuronal Synaptic Plasticity Regulation Of Astrocyte Differentiation Positive Regulation Of Adenosine Receptor Signaling Pathway Dendrite Self-avoidance Protein Localization To Juxtaparanode Region Of Axon Establishment Of Protein Localization To Juxtaparanode Region Of Axon Presynaptic Membrane Organization
Pathways		A tetrasaccharide linker sequence is required for GAG synthesis Chondroitin sulfate biosynthesis Dermatan sulfate biosynthesis CS/DS degradation ECM proteoglycans Defective B4GALT7 causes EDS, progeroid type Defective B3GAT3 causes JDSSDHD Defective CHST3 causes SEDCJD Defective CHST14 causes EDS, musculocontractural type Defective CHSY1 causes TPBS L1CAM interactions NCAM1 interactions Defective B3GALT6 causes EDSP2 and SEMDJL1	L1CAM interactions NCAM1 interactions NrCAM interactions
Drugs		Beta-D-Glucose Thiodigalactoside Hyaluronic acid
Diseases
GWAS		Bipolar disorder ( 24618891 31043756 21353194) Bipolar I disorder ( 31043756) Bipolar II disorder ( 31043756) C-reactive protein levels or LDL-cholesterol levels (pleiotropy) ( 27286809) C-reactive protein levels or total cholesterol levels (pleiotropy) ( 27286809) Cholesterol, total ( 19060911 26780889) LDL cholesterol ( 18193043 19060906 19060911 26780889) Nonalcoholic fatty liver disease ( 29385134) Schizophrenia ( 25056061 29483656 23974872) Triglycerides ( 18193043 19060906 19060911)	Adventurousness ( 30643258) Blood protein levels ( 30072576 29875488 28240269) Mean platelet volume ( 24026423) Number of sexual partners ( 30643258) Red blood cell count ( 27863252) Schizophrenia ( 30285260)
Interacting Genes		7 interacting genes: CNTN2 HMGB1 L1CAM NCAM1 PTN TNC TNR	11 interacting genes: CDK4 CHEK1 CNTN1 CNTNAP2 EGFR L1CAM NCAN NFYB NRCAM TUBG1 VAC14
Entrez ID		1463	6900
HPRD ID		02897	01826
Ensembl ID		ENSG00000130287	ENSG00000184144
Uniprot IDs		A0A024R7M3 O14594 Q4LE67	A1L3A3 A1ML24 Q02246
PDB IDs			2OM5
Enriched GO Terms of Interacting Partners?
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