ACOT8 - acyl-CoA thioesterase 8 Gene

Homo sapiens

Also known as hTE; NAP1; PTE1; PTE2; PTE-1; PTE-2; HNAACTE; hACTE-III

Gene ID: 10005 | Gene type: protein coding

About ACOT8

Cytogenetic location: 20q13.12 Genomic coordinates (GRCh38): 20:45,841,721-45,857,392 (from NCBI)

This gene has 13 transcripts (splice variants) and 202 orthologues. Ubiquitous expression in adrenal (RPKM 10.6), brain (RPKM 10.3) and 25 other tissues.

Summary

The protein encoded by this gene is a peroxisomal thioesterase that appears to be involved more in the oxidation of fatty acids rather than in their formation. The encoded protein can bind to the human immunodeficiency virus-1 protein Nef, and mediate Nef-induced down-regulation of CD4 in T-cells. [provided by RefSeq, Oct 2010]

ACOT8 Products(1)

mRNA	Protein	Name
NM_005469.4	NP_005460.2	acyl-coenzyme A thioesterase 8

ACOT8 Protein Structure

4HBT_3

0
100
200
300
319 a.a.

Protein Preferred Names

Protein Names

acyl-coenzyme A thioesterase 8

HIV-Nef associated acyl-CoA thioesterase

Related Diseases

Diseases

Alias

Non-Syndromic X-Linked Intellectual Disability 14

Mrx14

Flinders Island Spotted Fever

Fisf	Thai Tick Typhus

Hypotrichosis 1

HYPT1	Hhs
Hts	Hypotrichosis Simplex
Hypotrichosis Simplex, Generalized, Hereditary	Hereditary Generalized Hypotrichosis Simplex
Generalized Hypothricosis Simplex	Hypotrichosis Simplex Hereditary
Hypotrichosis, Type 1

Alpha-Methylacyl-Coa Racemase Deficiency

Amacr Deficiency

AMACRD

Peroxisomal Biogenesis Disorder

Zellweger Spectrum Disorders	Peroxisome Biogenesis Disorder-Zellweger Syndrome Spectrum
Disorders Of Peroxisome Biogenesis	Zellweger Spectrum
Zellweger Syndrome Spectrum	Peroxisomal Biogenesis Disorders
Pbd, Zss	Pbd-Zsd
Pbd-Zss	Pbd-Zellweger Spectrum Disorder
Peroxisomal Biogenesis Disorders, Zellweger Syndrome Spectrum	Peroxisome Biogenesis Disorder
Peroxisome Biogenesis Disorder Spectrum	Peroxisome Biogenesis Disorders
Zellweger Spectrum Disorder	Hyperpipecolic Acidaemia

Zellweger Syndrome

Cerebrohepatorenal Syndrome	Zellweger Leukodystrophy
Zs	Congenital Iron Overload
Chr	Zws
Severe Pbd-Zsd	Severe Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder

Non-Syndromic X-Linked Intellectual Disability

X-Linked Non-Syndromic Intellectual Disability	Non-Specific X-Linked Mental Retardation
X-Linked Non-Specific Intellectual Disability

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-RS00180	ACOT8 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	ACOT8	VGNC	VGNC:37519
Felis catus	ACOT8	VGNC	VGNC:59520
Bos taurus	ACOT8	VGNC	VGNC:25550
Rattus norvegicus	ACOT8	RGD	RGD:70368
Macaca mulatta	ACOT8	VGNC	VGNC:69413
Mus musculus	ACOT8	MGD	MGI:2158201

Name
Email *

	Sorry, but the email address you supplied was invalid.