SLC27A6 - solute carrier family 27 member 6 Gene

Also Known as FATP6; ACSVL2; FACVL2; VLCS-H1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 28965

About SLC27A6

Cytogenetic location: 5q23.3 Genomic coordinates (GRCh38): 5:128,965,488-129,033,635 (from NCBI)

This gene has 4 transcripts (splice variants), 227 orthologues and 12 paralogues. Biased expression in adrenal (RPKM 12.7), heart (RPKM 7.8) and 8 other tissues.

Summary

This gene encodes a member of the fatty acid transport protein family (FATP). FATPs are involved in the uptake of long-chain fatty acids and have unique expression patterns. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

SLC27A6 Products (3)

mRNA Protein Name
NM_001017372.3 NP_001017372.1 long-chain fatty acid transport protein 6
NM_001317984.2 NP_001304913.1 long-chain fatty acid transport protein 6
NM_014031.5 NP_054750.1 long-chain fatty acid transport protein 6

SLC27A6 Protein Structure

AMP-binding

AMP-binding: AMP-binding enzyme (61 - 486)

AMP-binding_C

AMP-binding_C: AMP-binding enzyme C-terminal domain (495 - 571)

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  • 500
  • 619 a.a.
Protein Preferred Names Protein Names

long-chain fatty acid transport protein 6

  • acyl-CoA synthetase very long chain family, member 2

Related Diseases

Diseases Alias
Lethal Restrictive Dermopathy

  • Hyperkeratosis-Contracture Syndrome

  • Tight Skin Contracture Syndrome

  • Tight Skin Contracture Syndrome, Lethal

  • Dermopathy, Restrictive, Lethal
Platelet Glycoprotein Iv Deficiency

  • Platelet-Type Bleeding Disorder 10

  • Bdplt10

  • Cd36 Deficiency

  • Bleeding Disorder, Platelet-Type, 10

  • PG4D

  • Bleeding Disorder Platelet-Type 10

  • Deficiency, Platelet Glycoprotein Iv
Melkersson-Rosenthal Syndrome

  • Melkersson Syndrome

  • Mros

  • Mrs

  • Cheilitis Granulomatosa Of Mescher-Melkersson-Rosenthal

  • Melkersson'S Syndrome

  • Cheilitis Granulomatosa

  • Granulomatous Cheilitis
Persistent Fetal Circulation Syndrome

  • Persistent Fetal Circulation

  • Fetal Circulation

  • Persistent Pulmonary Hypertension Of The Newborn

  • Congenital Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins

  • Persistent Foetal Circulation

  • Persistent Foetal Circulation Syndrome

  • Pfc - [Persistent Fetal Circulation] Syndrome

  • Pphn - [Persistent Pulmonary Hypertension Of The Newborn]

  • Newborn Pulmonary Hypertension

  • Primary Pulmonary Hypertension Of Newborn
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Art. -Nr. Produktname
Wirkung
Reinheit
Rare Diseases
HY-RS13149 SLC27A6 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris SLC27A6 VGNC VGNC:46333
Bos taurus SLC27A6 VGNC VGNC:34790
Mus musculus SLC27A6 MGD MGI:3036230
Macaca mulatta SLC27A6 VGNC VGNC:77443
Felis catus SLC27A6 VGNC VGNC:65293
Rattus norvegicus SLC27A6 RGD RGD:1311977
Others SLC27A6 NCBI