Human (GRCh37.p13)
Description

complement component 2 [Source:HGNC Symbol;Acc:1248]

Gene Synonyms

ARMD14, CO2

Location

Chromosome 6: 31,865,562-31,913,449 forward strand.

GRCh37:CM000668.1

View alleles of this gene on alternative sequences

About this gene

This gene has 17 transcripts (splice variants), 1 gene allele, 2 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000299367.5C2-0012850752aaENSP00000299367.5
 
Protein coding
CCDS4728P06681 Q5JP69 Q5ST52
Q6LDG4 Q95IG1
NM_000063.4Ensembl CanonicalGENCODE Basic
ENST00000442278.2C2-0102434620aaENSP00000395683.2
 
Protein coding
CCDS54991P06681 Q6LDG4 NM_001145903.1GENCODE Basic
ENST00000452323.2C2-0141999538aaENSP00000392322.2
 
Protein coding
CCDS56416P06681 NM_001178063.1GENCODE Basic
ENST00000469372.1C2-0171906506aaENSP00000418923.1
 
Protein coding
B4DQI1 NM_001282457.1GENCODE Basic
ENST00000383177.3C2-0031847526aaENSP00000372664.3
 
Protein coding
--CDS 5' incomplete
ENST00000418949.2C2-0021658328aaENSP00000406190.2
 
Protein coding
Q5ST52 Q8N6L6 NM_001282459.1GENCODE Basic
ENST00000497706.1C2-0041609463aaENSP00000417482.1
 
Protein coding
B3KTX9 E9PDZ0 -CDS 3' incomplete
ENST00000447952.2C2-009837203aaENSP00000391354.2
 
Protein coding
F2Z3N2 -CDS 3' incomplete
ENST00000413154.1C2-007561139aaENSP00000403325.1
 
Protein coding
Q5ST52 -CDS 3' incomplete
ENST00000452202.1C2-015539158aaENSP00000406121.1
 
Protein coding
A2ABG0 -CDS 3' incomplete
ENST00000494905.1C2-011536136aaENSP00000419048.1
 
Protein coding
C9JYQ5 -CDS 3' incomplete
ENST00000482060.1C2-0182335104aaENSP00000418332.1
 
Nonsense mediated decay
F8WCJ9 --
ENST00000485690.1C2-012894160aaENSP00000417790.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000411571.2C2-00677384aaENSP00000388727.2
 
Nonsense mediated decay
F2Z306 --
ENST00000484636.1C2-00854284aaENSP00000420305.1
 
Nonsense mediated decay
F2Z306 --
ENST00000468407.1C2-013694No protein-
 
Processed transcript
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ENST00000486124.1C2-0052800No protein-
 
Retained intron
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