C2

GENERAL INFORMATION

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Gene name

C2

Gene description

Complement component 2

Protein class

Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted intracellular proteins
Predicted secreted proteins

Predicted localization

Intracellular,Secreted

Number of transcripts

11
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (liver)
GTEx:Tissue enhanced (liver)

Protein evidence

Evidence at protein level

Protein localization

Positivity in plasma.

ANTIBODY RELIABILITY

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Data reliability
description

Secreted protein, tissue location of RNA and protein might differ and correlation is complex.

Data reliability

Supportive based on 1 antibody.
CAB016775
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (liver)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (liver)

Organ

Expression



GENE INFORMATION

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Gene name

C2

Synonyms

Description

Complement component 2 (HGNC Symbol)

Entrez gene summary

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]

Chromosome

6

Cytoband

p21.33

Chromosome location (bp)

31897785 - 31945672

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000166278 (version 78.38)

Entrez gene

717

UniProt

P06681 (UniProt - Evidence at protein level)

neXtProt

NX_P06681

Antibodypedia

C2 antibodies


PROTEIN BROWSER

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ENST00000299367
 
ENST00000383177
 
ENST00000413154
 
ENST00000418949
 
ENST00000442278
 
ENST00000447952
 
ENST00000452202
 
ENST00000452323
 
ENST00000469372
 
ENST00000494905
 
ENST00000497706
 
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PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

C2-001 ENSP00000299367
ENST00000299367
P06681
Show all »
Show » Show » 752 83.3 Yes 0
C2-002 ENSP00000406190
ENST00000418949
Q8N6L6
Show all »
Show » 328 35.5 Yes 0
C2-003 ENSP00000372664
ENST00000383177
Show » Show » 526 58.8 Yes 0
C2-004 ENSP00000417482
ENST00000497706
E9PDZ0
Show all »
Show » Show » 463 51.4 No 0
C2-007 ENSP00000403325
ENST00000413154
Q5ST52
Show all »
Show » 139 14.8 Yes 0
C2-009 ENSP00000391354
ENST00000447952
F2Z3N2
Show all »
Show » 203 21.7 Yes 0
C2-010 ENSP00000395683
ENST00000442278
P06681
Show all »
Show » Show » 620 69.4 Yes 0
C2-011 ENSP00000419048
ENST00000494905
C9JYQ5
Show all »
Show » 136 14.9 No 0
C2-014 ENSP00000392322
ENST00000452323
P06681
Show all »
Show » Show » 538 60.3 No 0
C2-015 ENSP00000406121
ENST00000452202
A2ABG0
Show all »
Show » 158 17.5 No 0
C2-017 ENSP00000418923
ENST00000469372
B4DQI1
Show all »
Show » Show » 506 56.5 No 0