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Very long-chain acyl-CoA synthetase

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(Redirected from SLC27A2) Protein-coding gene in the species Homo sapiens
SLC27A2
Identifiers
AliasesSLC27A2, ACSVL1, FACVL1, FATP2, HsT17226, VLACS, VLCS, hFACVL1, solute carrier family 27 member 2
External IDsOMIM: 603247; MGI: 1347099; HomoloGene: 37830; GeneCards: SLC27A2; OMA:SLC27A2 - orthologs
EC number6.2.1.3
Gene location (Human)
Chromosome 15 (human)
Chr.Chromosome 15 (human)
Chromosome 15 (human)Genomic location for SLC27A2Genomic location for SLC27A2
Band15q21.2Start50,182,196 bp
End50,236,385 bp
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)
Chromosome 2 (mouse)Genomic location for SLC27A2Genomic location for SLC27A2
Band2|2 F1Start126,394,327 bp
End126,430,163 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • bronchial epithelial cell

  • liver

  • right lobe of liver

  • kidney tubule

  • corpus epididymis

  • mucosa of transverse colon

  • caput epididymis

  • mucosa of paranasal sinus

  • glomerulus

  • metanephric glomerulus
Top expressed in
  • right kidney

  • proximal tubule

  • human kidney

  • left lobe of liver

  • saccule

  • olfactory epithelium

  • parotid gland

  • Paneth cell

  • gallbladder

  • lacrimal gland
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

11001

26458

Ensembl

ENSG00000140284

ENSMUSG00000027359

UniProt

O14975

O35488

RefSeq (mRNA)

NM_003645
NM_001159629

NM_011978

RefSeq (protein)

NP_001153101
NP_003636

NP_036108

Location (UCSC)Chr 15: 50.18 – 50.24 MbChr 2: 126.39 – 126.43 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Very long-chain acyl-CoA synthetase is an enzyme that in humans is encoded by the SLC27A2 gene.

The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very long chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney and is present in both endoplasmic reticulum and peroxisomes but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000140284Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000027359Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Wakui K, Aoyama T, Uchiyama A, Hashimoto T, Fukushima Y (Oct 1998). "Assignment of human fatty-acid-coenzyme A ligase, very long-chain 1 gene (FACVL1) to human chromosome band 15q21.2 by fluorescence in situ hybridization". Cytogenet Cell Genet. 81 (3–4): 292–3. doi:10.1159/000015051. PMID 9730624. S2CID 46774274.
  6. ^ "Entrez Gene: SLC27A2 solute carrier family 27 (fatty acid transporter), member 2".

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Membrane proteins, carrier proteins: membrane transport proteins solute carrier (TC 2A)
By group
SLC1–10
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SLC11–20
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SLC21–30
(21):
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SLC31–40
(31):
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SLC41–48
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SLCO1–4
Ion pumps
Symporter, Cotransporter
Antiporter (exchanger)
see also solute carrier disorders
Peroxisomal and lysosomal proteins
Enzymes
Transporters
Structure/Peroxin
LAMP
see also intermediates, disorders


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