Human (GRCh37.p13)
Description

solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 [Source:HGNC Symbol;Acc:10986]

Gene Synonyms

D10S105E, GDA, GDC, HGT.1, ML7, hML7

Location

Chromosome 10: 70,237,756-70,287,231 reverse strand.

GRCh37:CM000672.1

About this gene

This gene has 8 transcripts (splice variants) and 6 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000609923.1SLC25A16-0026529332aaENSP00000476815.1
 
Protein coding
CCDS7280B4DPV4 P16260 NM_152707.3GENCODE basic
ENST00000539557.1SLC25A16-2011644234aaENSP00000443914.1
 
Protein coding
B4DPV4 -GENCODE basic
ENST00000608053.1SLC25A16-00726365aaENSP00000477328.1
 
Protein coding
--CDS 5' incomplete
ENST00000493963.1SLC25A16-003112157aaENSP00000476283.1
 
Nonsense mediated decay
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ENST00000491102.2SLC25A16-00553892aaENSP00000476555.1
 
Nonsense mediated decay
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ENST00000474927.1SLC25A16-00431165aaENSP00000476587.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000265870.3SLC25A16-0012295No protein-
 
Processed transcript
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ENST00000439904.3SLC25A16-0061779No protein-
 
Processed transcript
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