C2 (complement C2)

2019-08-01  

Identity

HGNC
LOCATION
6p21.33
LOCUSID
ALIAS
ARMD14,CO2

Other Information

Locus ID:

NCBI: 717
MIM: 613927
HGNC: 1248
Ensembl: ENSG00000166278

Variants:

dbSNP: 717
ClinVar: 717
TCGA: ENSG00000166278
COSMIC: C2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000166278ENST00000299367P06681
ENSG00000166278ENST00000299367Q5JP69
ENSG00000166278ENST00000383177H0Y3H6
ENSG00000166278ENST00000411571F2Z306
ENSG00000166278ENST00000413154Q5ST52
ENSG00000166278ENST00000418949Q8N6L6
ENSG00000166278ENST00000442278P06681
ENSG00000166278ENST00000447952F2Z3N2
ENSG00000166278ENST00000452202A2ABG0
ENSG00000166278ENST00000452323P06681
ENSG00000166278ENST00000469372B4DQI1
ENSG00000166278ENST00000482060F8WCJ9
ENSG00000166278ENST00000484636F2Z306
ENSG00000166278ENST00000485690H0Y868
ENSG00000166278ENST00000494905C9JYQ5
ENSG00000166278ENST00000497706E9PDZ0

Expression (GTEx)

0
50
100
150
200

Pathways

PathwaySourceExternal ID
Complement and coagulation cascadesKEGGko04610
Systemic lupus erythematosusKEGGko05322
Complement and coagulation cascadesKEGGhsa04610
Systemic lupus erythematosusKEGGhsa05322
Staphylococcus aureus infectionKEGGko05150
Staphylococcus aureus infectionKEGGhsa05150
PertussisKEGGko05133
PertussisKEGGhsa05133
Immune SystemREACTOMER-HSA-168256
Innate Immune SystemREACTOMER-HSA-168249
Complement cascadeREACTOMER-HSA-166658
Initial triggering of complementREACTOMER-HSA-166663
Activation of C3 and C5REACTOMER-HSA-174577
Regulation of Complement cascadeREACTOMER-HSA-977606

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
361942492023Proteomic analysis of diabetes genetic risk scores identifies complement C2 and neuropilin-2 as predictors of type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) Study.2
361942492023Proteomic analysis of diabetes genetic risk scores identifies complement C2 and neuropilin-2 as predictors of type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) Study.2
348996882021Gain-of-Function Mutations R249C and S250C in Complement C2 Protein Increase C3 Deposition in the Presence of C-Reactive Protein.7
348996882021Gain-of-Function Mutations R249C and S250C in Complement C2 Protein Increase C3 Deposition in the Presence of C-Reactive Protein.7
321643492020Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family.0
329133452020Complement protein levels and MBL2 polymorphisms are associated with dengue and disease severity.7
321643492020Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family.0
329133452020Complement protein levels and MBL2 polymorphisms are associated with dengue and disease severity.7
292834942018Genetic association of complement component 2 variants with chronic hepatitis B in a Korean population.3
301795272018Association Between Complement Factor C2/C3/CFB/CFH Polymorphisms and Age-Related Macular Degeneration: A Meta-Analysis.20
292834942018Genetic association of complement component 2 variants with chronic hepatitis B in a Korean population.3
301795272018Association Between Complement Factor C2/C3/CFB/CFH Polymorphisms and Age-Related Macular Degeneration: A Meta-Analysis.20
287421392017Acquisition of C1 inhibitor by Bordetella pertussis virulence associated gene 8 results in C2 and C4 consumption away from the bacterial surface.22
287421392017Acquisition of C1 inhibitor by Bordetella pertussis virulence associated gene 8 results in C2 and C4 consumption away from the bacterial surface.22
272523792016Solution Structures of Complement C2 and Its C4 Complexes Propose Pathway-specific Mechanisms for Control and Activation of the Complement Proconvertases.15

Citation

Dessen P

C2 (complement C2)

Atlas Genet Cytogenet Oncol Haematol. 2019-08-01

Online version: http://atlasgeneticsoncology.org/gene/58120/c2-(complement-c2)