SLC27A5

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Bile acyl-CoA synthetase is an enzyme that in humans is encoded by the SLC27A5 gene.[5][6][7]

AliasesSLC27A5, ACSB, ACSVL6, BACS, BAL, FACVL3, FATP-5, FATP5, VLACSR, VLCS-H2, VLCSH2, solute carrier family 27 member 5
End58,512,413 bp[1]
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SLC27A5
Identifiers
AliasesSLC27A5, ACSB, ACSVL6, BACS, BAL, FACVL3, FATP-5, FATP5, VLACSR, VLCS-H2, VLCSH2, solute carrier family 27 member 5
External IDsOMIM: 603314; MGI: 1347100; HomoloGene: 7596; GeneCards: SLC27A5; OMA:SLC27A5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012254
NM_001321196

NM_009512

RefSeq (protein)

NP_001308125
NP_036386

NP_033538

Location (UCSC)Chr 19: 58.48 – 58.51 MbChr 7: 12.72 – 12.73 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene is an isozyme of very long-chain acyl-CoA synthetase (VLCS). It is capable of activating very long-chain fatty-acids containing 24- and 26-carbons. It is expressed in liver and associated with endoplasmic reticulum but not with peroxisomes. Its primary role is in fatty acid elongation or complex lipid synthesis rather than in degradation. This gene has a mouse ortholog.[7]

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References

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