SLC27A6 - solute carrier family 27 member 6 Gene

Homo sapiens

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

Gene ID: 28965 | Gene type: protein coding

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_C

0
100
200
300
400
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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13149	SLC27A6 Human Pre-designed siRNA Set A		/	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

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