SLC27A2 - solute carrier family 27 member 2 Gene

Also Known as VLCS; FATP2; VLACS; ACSVL1; FACVL1; hFACVL1; HsT17226

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 11001

About SLC27A2

Cytogenetic location: 15q21.2 Genomic coordinates (GRCh38): 15:50,182,196-50,236,385 (from NCBI)

This gene has 4 transcripts (splice variants), 184 orthologues and 12 paralogues. Biased expression in liver (RPKM 63.2), kidney (RPKM 62.8) and 5 other tissues.

Summary

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. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]

SLC27A2 Products (2)

mRNA Protein Name
NM_001159629.2 NP_001153101.1 long-chain fatty acid transport protein 2 isoform 2
NM_003645.4 NP_003636.2 long-chain fatty acid transport protein 2 isoform 1
Molecular Function GO Annotation Evidence Verweise Source
enables enzyme binding IPI
IPI: Inferred from physical interaction
16781659 GOA
enables long-chain fatty acid transmembrane transporter activity IDA
IDA: Inferred from direct assay
20530735 GOA
enables long-chain fatty acid-CoA ligase activity IDA
IDA: Inferred from direct assay
10198260 GOA
enables phytanate-CoA ligase activity IDA
IDA: Inferred from direct assay
10198260 GOA
enables pristanate-CoA ligase activity IDA
IDA: Inferred from direct assay
10198260 GOA
enables very long-chain fatty acid-CoA ligase activity IDA
IDA: Inferred from direct assay
10198260 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in bile acid biosynthetic process IDA
IDA: Inferred from direct assay
11980911 GOA
involved in fatty acid alpha-oxidation IDA
IDA: Inferred from direct assay
10198260 GOA
involved in fatty acid beta-oxidation IDA
IDA: Inferred from direct assay
10198260 GOA
acts upstream of long-chain fatty acid import into cell IDA
IDA: Inferred from direct assay
22022213 GOA
involved in long-chain fatty acid metabolic process IDA
IDA: Inferred from direct assay
22022213 GOA
involved in methyl-branched fatty acid metabolic process IDA
IDA: Inferred from direct assay
10198260 GOA
Cellular Component GO Annotation Evidence Verweise Source
located in endoplasmic reticulum lumen IDA
IDA: Inferred from direct assay
10198260 GOA
located in endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
11980911 GOA
located in peroxisomal membrane IDA
IDA: Inferred from direct assay
10198260 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC27A2 Protein Structure

AMP-binding

AMP-binding: AMP-binding enzyme (59 - 487)

AMP-binding_C

AMP-binding_C: AMP-binding enzyme C-terminal domain (496 - 572)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 620 a.a.
Protein Preferred Names Protein Names

long-chain fatty acid transport protein 2

  • FATP-2

SLC27A2 Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P83821 SLC27A2 Antibody (YA3518) IHC-P, ELISA Human
HY-P83821A SLC27A2 Antibody (YA3518)(PBS only) IHC-P, ELISA Human

Related Diseases

Diseases Alias
Adrenoleukodystrophy
  • X-Linked Adrenoleukodystrophy

  • ALD

  • Siemerling-Creutzfeldt Disease

  • X-Ald

  • X-Linked Cerebral Adrenoleukodystrophy

  • Bronze Schilder Disease

  • Melanodermic Leukodystrophy

  • Addison Disease And Cerebral Sclerosis

  • Adrenomyeloneuropathy, Adult

  • Diffuse Sclerosis

  • X-Cald

  • Adrenomyeloneuropathy

  • Encephalitis Periaxialis Concentrica

  • Encephalitis Periaxialis, Schilder'S

  • Sudanophilic Cerebral Sclerosis

  • Ald Childhood Cerebral Form

  • Adrenoleukodystrophy X-Linked Cerebral Form

  • Adrenoleukodystrophy Childhood Cerebral Form

  • Childhood Cerebral Ald

  • Schilder Disease

  • X-Linked Ald

  • Adrenoleukodystrophy, X-Linked

  • Amn

  • Diffuse Cerebral Sclerosis Of Schilder

  • Systemic Scleroderma

  • Balo'S Concentric Sclerosis

  • Ald - [Adrenoleukodystrophy]

  • Addison-Schilder

Zellweger Syndrome
  • Cerebrohepatorenal Syndrome

  • Zellweger Leukodystrophy

  • Zs

  • Congenital Iron Overload

  • Chr

  • Zws

  • Severe Pbd-Zsd

  • Severe Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris SLC27A2 VGNC VGNC:46330
Felis catus SLC27A2 VGNC VGNC:65289
Bos taurus SLC27A2 VGNC VGNC:34786
Mus musculus SLC27A2 MGD MGI:1347099
Macaca mulatta SLC27A2 VGNC VGNC:77439
Rattus norvegicus SLC27A2 RGD RGD:71103
Others SLC27A2 NCBI