Human (GRCh37.p13)
Description

solute carrier family 16, member 4 [Source:HGNC Symbol;Acc:10925]

Gene Synonyms

MCT4, MCT5

Location

Chromosome 1: 110,905,470-110,933,704 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 10 transcripts (splice variants) and 11 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000369779.4SLC16A4-0012632487aaENSP00000358794.4
 
Protein coding
CCDS823O15374 NM_004696.2Ensembl CanonicalGENCODE basic
ENST00000472422.2SLC16A4-0022420439aaENSP00000432495.1
 
Protein coding
CCDS55623O15374 NM_001201546.1GENCODE basic
ENST00000369781.4SLC16A4-0042082319aaENSP00000358796.4
 
Protein coding
CCDS55624O15374 NM_001201549.1GENCODE basic
ENST00000541986.1SLC16A4-2021551425aaENSP00000446087.1
 
Protein coding
CCDS55622O15374 -GENCODE basic
ENST00000437429.2SLC16A4-2011541382aaENSP00000394790.2
 
Protein coding
CCDS55621O15374 NM_001201548.1GENCODE basic
ENST00000467986.2SLC16A4-0071059219aaENSP00000435768.1
 
Protein coding
H0YEG4 -CDS 5' incomplete
ENST00000461647.2SLC16A4-003196257aaENSP00000432190.1
 
Nonsense mediated decay
E9PKZ1 --
ENST00000528649.1SLC16A4-006156242aaENSP00000434136.1
 
Nonsense mediated decay
E9PRV1 --
ENST00000492412.2SLC16A4-008155157aaENSP00000433463.1
 
Nonsense mediated decay
E9PKZ1 --
ENST00000497687.1SLC16A4-005783No protein-
 
Processed transcript
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