Human (GRCh37.p13)
Description

solute carrier family 27 (fatty acid transporter), member 5 [Source:HGNC Symbol;Acc:10999]

Gene Synonyms

ACSB, ACSVL6, BACS, BAL, FACVL3, FATP-5, FATP5, FLJ22987, VLACSR, VLCS-H2, VLCSH2

Location

Chromosome 19: 58,990,879-59,023,780 reverse strand.

GRCh37:CM000681.1

About this gene

This gene has 8 transcripts (splice variants), 5 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000263093.2SLC27A5-0012361690aaENSP00000263093.2
 
Protein coding
CCDS12983M0R075 Q9Y2P5 NM_012254.2GENCODE basic
ENST00000601355.1SLC27A5-0021987606aaENSP00000470368.1
 
Protein coding
B4DPQ1 M0R075 -GENCODE basic
ENST00000594786.1SLC27A5-00464395aaENSP00000471065.1
 
Protein coding
M0R075 -GENCODE basic
ENST00000595851.1SLC27A5-008200395aaENSP00000469512.1
 
Nonsense mediated decay
M0R075 --
ENST00000599700.1SLC27A5-005474No protein-
 
Processed transcript
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ENST00000593745.1SLC27A5-0075032No protein-
 
Retained intron
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ENST00000601997.1SLC27A5-006575No protein-
 
Retained intron
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ENST00000594683.1SLC27A5-003564No protein-
 
Retained intron
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