Human (GRCh37.p13)
Description

chromosome 12 open reading frame 4 [Source:HGNC Symbol;Acc:1184]

Location

Chromosome 12: 4,596,894-4,647,674 reverse strand.

GRCh37:CM000674.1

About this gene

This gene has 9 transcripts (splice variants) and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000261250.3C12orf4-0013826552aaENSP00000261250.3
 
Protein coding
CCDS8528F5GXX6 F5H744 Q9NQ89
NM_020374.2GENCODE basic
ENST00000545746.1C12orf4-0022168552aaENSP00000439996.1
 
Protein coding
CCDS8528F5GXX6 F5H744 Q9NQ89
-GENCODE basic
ENST00000541014.1C12orf4-0051049204aaENSP00000440820.1
 
Protein coding
F5GXX6 -CDS 3' incomplete
ENST00000542080.1C12orf4-004561144aaENSP00000442806.1
 
Protein coding
F5H744 -CDS 3' incomplete
ENST00000544258.1C12orf4-00872747aaENSP00000444594.1
 
Nonsense mediated decay
H0YGS6 -CDS 5' incomplete
ENST00000544697.1C12orf4-00668577aaENSP00000439471.1
 
Nonsense mediated decay
F5H271 --
ENST00000509318.2C12orf4-009574No protein-
 
Processed transcript
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ENST00000535887.1C12orf4-007568No protein-
 
Retained intron
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ENST00000535030.1C12orf4-003561No protein-
 
Retained intron
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