Human (GRCh37.p13)
Description

family with sequence similarity 134, member A [Source:HGNC Symbol;Acc:28450]

Gene Synonyms

C2orf17, MGC3035

Location

Chromosome 2: 220,040,947-220,050,201 forward strand.

GRCh37:CM000664.1

About this gene

This gene has 10 transcripts (splice variants) and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000430297.2FAM134A-0014618543aaENSP00000395249.2
 
Protein coding
CCDS2434C9J3K5 C9JIF3 Q8NC44
NM_024293.4GENCODE basic
ENST00000420189.1FAM134A-0041781203aaENSP00000411247.1
 
Protein coding
--CDS 5' incomplete
ENST00000458520.1FAM134A-005992167aaENSP00000403898.1
 
Protein coding
C9J3K5 C9JIF3 -CDS 3' incomplete
ENST00000452022.1FAM134A-00972994aaENSP00000391284.1
 
Protein coding
C9J3K5 -CDS 3' incomplete
ENST00000430747.1FAM134A-0085635aaENSP00000399261.1
 
Protein coding
--CDS 3' incomplete
ENST00000443757.1FAM134A-0065585aaENSP00000414547.1
 
Protein coding
--CDS 3' incomplete
ENST00000273048.2FAM134A-0022533178aaENSP00000273048.2
 
Nonsense mediated decay
F8WAL5 --
ENST00000452293.1FAM134A-007609102aaENSP00000394606.1
 
Nonsense mediated decay
F8WE68 --
ENST00000465672.1FAM134A-010550No protein-
 
Retained intron
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ENST00000481925.1FAM134A-011543No protein-
 
Retained intron
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