Human (GRCh38.p14)
Description

solute carrier family 16 member 8 [Source:HGNC Symbol;Acc:HGNC:16270]

Gene Synonyms

MCT3, REMP

Location

Chromosome 22: 38,078,134-38,084,184 reverse strand.

GRCh38:CM000684.2

About this gene

This gene has 9 transcripts (splice variants), 169 orthologues and 13 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000681075.2SLC16A8-2042291504aaENSP00000506669.1
 
Protein coding
CCDS13966O95907 NM_013356.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000902580.1SLC16A8-2052123504aaENSP00000572639.1
 
Protein coding
CCDS13966--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000320521.10SLC16A8-2012091504aaENSP00000321735.5
 
Protein coding
CCDS13966O95907 -GENCODE BasicAPPRIS P1TSL:1
ENST00000902582.1SLC16A8-2071229224aaENSP00000572641.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000902584.1SLC16A8-2091198224aaENSP00000572643.1
 
Protein coding
--GENCODE Basic
ENST00000902581.1SLC16A8-2061131176aaENSP00000572640.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000902583.1SLC16A8-2081083176aaENSP00000572642.1
 
Protein coding
--GENCODE Basic
ENST00000469516.5SLC16A8-203677No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000427592.2SLC16A8-202497No protein-
 
Retained intron
--TSL:3