Complement Component C2 Products

Description

Complement C2 functions as part of the classical pathway complement system. Lack of complement C2 has been linked with some autoimmune diseases and recurrent/invasive infections. This protein is known to have interactions with C3, C4B, C5, PSMA4 and MASP1.

Bioinformatics

Entrez	717 Human
Uniprot	AAH29781 Human NM_000063 Human NP_000054.2 Human P06681 Human
Product By Gene ID	717
Alternate Names	C3/C5 convertase CO2 complement C2 complement component 2 complement component C2 DKFZp779M0311 EC 3.4.21 EC 3.4.21.43

Diseases related to Complement Component C2

Discover more about diseases related to Complement Component C2.

Neoplasms
Fracture
Pain
Malignant Neoplasms
Carcinoma
Dislocations
Infective Disorder
Spinal Fractures
Spinal Cord Injuries
Neck Pain
Hiv Infections
Disease Of Adrenal Medulla
Hemorrhage
Immunologic Deficiency Syndromes
Lupus Erythematosus, Systemic
Flexed Fetal Attitude
Hemolysis (disorder)
Headache
Fracture Of First Cervical Vertebra
Inflammation

Pathways for Complement Component C2

View related products by pathway and learn more about each of the pathways below.

Transport
Localization
Pathogenesis
Secretion
Complement Activation
Coagulation
Translation
Reflex
Cell Death
Proteolysis
Cell Cycle
Immune Response
Cell Proliferation
Fermentation
Glycosylation
Innervation
Cell Growth
Ossification
Methylation
Virulence

PTMs for Complement Component C2

Learn more about PTMs related to Complement Component C2.

Cleavage
Phosphorylation
Oxidation
Ribosylation
Glycosylation
Methylation
Reduction
Carboxylation
Hydroxylation
Nitration
Acetylation
Decarboxylation
Ubiquitination
Dephosphorylation
Biotinylation
Acylation
Amination
Deamination
Deglycosylation
Bromination

Bioinformatics Tool for Complement Component C2

Discover related pathways, diseases and genes to Complement Component C2. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.