Mus musculus Gene: C2
Summary
InnateDB Gene IDBG-174547.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C2
Gene Name complement component 2 (within H-2S)
Synonyms
Species Mus musculus
Ensembl Gene ENSMUSG00000024371
Encoded Proteins
complement component 2 (within H-2S)
complement component 2 (within H-2S)
complement component 2 (within H-2S)
complement component 2 (within H-2S)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation from Orthologs
Summary
[Homo sapiens] Staphylococcus aureus extracellular adherence protein (Eap) binds to C4B to inhibit binding of both full-length C2 and its C2b fragment, disrupting the formation of the C3 proconvertase (C4b2) and significantly diminishing the extent of S. aureus opsonophagocytosis and killing by neutrophils.
[Homo sapiens] Complement interfering protein (CIP) of group B Streptococcus (GBS) shows high affinity toward C4B and inhibits its interaction with C2, presumably preventing the formation of the C4BC2A convertase and GBS phagocytic killing in the absence of anti-GBS antibodies.
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000166278:
Component C2 is a serum glycoprotein that functions as part of the classical pathway of the complement system. Activated C1 cleaves C2 into C2a and C2b. The serine proteinase C2a then combines with complement factor 4b to create the C3 or C5 convertase. Deficiency of C2 has been reported to associated with certain autoimmune diseases and SNPs in this gene have been associated with altered susceptibility to age-related macular degeneration. This gene localizes within the class III region of the MHC on the short arm of chromosome 6. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described in publications but their full-length sequence has not been determined.[provided by RefSeq, Mar 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 17:34862604-34898265
Strand Reverse strand
Band B1
Transcripts
ENSMUST00000025230 ENSMUSP00000025230
ENSMUST00000152417 ENSMUSP00000123536
ENSMUST00000148431 ENSMUSP00000120009
ENSMUST00000134300 ENSMUSP00000114241
ENSMUST00000127795
ENSMUST00000130728
ENSMUST00000174880
ENSMUST00000174279
ENSMUST00000176332 ENSMUSP00000135304
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 6 interaction(s) predicted by orthology.
Predicted by orthology
Total 6 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004252 serine-type endopeptidase activity
GO:0005515 protein binding
Biological Process
GO:0006508 proteolysis
GO:0006956 complement activation
GO:0006958 complement activation, classical pathway
GO:0007584 response to nutrient
GO:0045087 innate immune response
GO:2000427 positive regulation of apoptotic cell clearance
Cellular Component
GO:0005576 extracellular region
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Innate Immune System pathway
Complement cascade pathway
Regulation of Complement cascade pathway
Immune System pathway
Initial triggering of complement pathway
Activation of C3 and C5 pathway
KEGG
Complement and coagulation cascades pathway
Systemic lupus erythematosus pathway
Staphylococcus aureus infection pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Activation of C3 and C5 pathway
Initial triggering of complement pathway
Regulation of Complement cascade pathway
Innate Immune System pathway
Immune System pathway
Complement cascade pathway
KEGG
Complement and coagulation cascades pathway
Systemic lupus erythematosus pathway
Staphylococcus aureus infection pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL B8JJN2 Q792Q3
UniProt Splice Variant
Entrez Gene 12263
UniGene Mm.283217 Mm.412910 Mm.472274
RefSeq NM_013484 NM_001142706 NM_008198 XM_006523671 XM_006523672 XM_006525304 XM_006525305 XM_006536523 XM_006536524 XM_006537256 XM_006537257
OMIM
CCDS CCDS28664 CCDS28663 CCDS50079
HPRD
IMGT
MGI ID MGI:88226
MGI Symbol C2
EMBL AF049850 CT025759
GenPept AAC05284
RNA Seq Atlas 12263