Human (GRCh38.p14)
Description

solute carrier family 16 member 2 [Source:HGNC Symbol;Acc:HGNC:10923]

Gene Synonyms

AHDS, DXS128, DXS128E, MCT7, MCT8, MRX22, XPCT

Location

Chromosome X: 74,421,493-74,533,917 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 3 transcripts (splice variants), 257 orthologues, 13 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000587091.6SLC16A2-2014128539aaENSP00000465734.1
 
Protein coding
CCDS14426P36021 NM_006517.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000590447.1SLC16A2-2021886229aaENSP00000466213.1
 
Protein coding
K7ELT4 -TSL:5CDS 5' incomplete
ENST00000636771.1SLC16A2-203389369aaENSP00000490445.1
 
Nonsense mediated decay
A0A1B0GVB4 -TSL:5CDS 5' incomplete