1. Gene
  2. ACOT13 - acyl-CoA thioesterase 13 Gene

ACOT13 - acyl-CoA thioesterase 13 Gene

Homo sapiens

Also known as HT012; THEM2; PNAS-27

Gene ID: 55856 | Gene type: protein coding

About ACOT13

Cytogenetic location: 6p22.3 Genomic coordinates (GRCh38): 6:24,667,077-24,705,046 (from NCBI)

This gene has 3 transcripts (splice variants) and 200 orthologues. Ubiquitous expression in kidney (RPKM 18.3), liver (RPKM 16.3) and 25 other tissues.

Summary

This gene encodes a member of the thioesterase superfamily. In humans, the protein co-localizes with microtubules and is essential for sustained cell proliferation. The orthologous mouse protein forms a homotetramer and is associated with mitochondria. The mouse protein functions as a medium- and long-chain acyl-CoA thioesterase. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2009]

ACOT13 Products(2)

mRNA Protein Name
NM_001160094.2 NP_001153566.1 acyl-coenzyme A thioesterase 13 isoform 2
NM_018473.4 NP_060943.1 acyl-coenzyme A thioesterase 13 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables fatty acyl-CoA hydrolase activity IDA
IDA: Inferred from direct assay
16934754 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence Reference Source
involved in protein homotetramerization IPI
IPI: Inferred from physical interaction
16934754 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

ACOT13 Protein Structure

4HBT

4HBT: Thioesterase superfamily (53 - 126)

  • 0
  • 100
  • 140 a.a.
Protein Preferred Names Protein Names

acyl-coenzyme A thioesterase 13

hotdog-fold thioesterase superfamily member 2

ACOT13 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
ACOT13 Q9NPJ3 YWHAG Homo sapiens P61981 32814053
Intra
ACOT13 Q9NPJ3 YWHAG Homo sapiens P61981 32814053
Intra
ACOT13 Q9NPJ3 YWHAG Homo sapiens P61981 32814053
Intra
ACOT13 Q9NPJ3 KAT5 Homo sapiens Q92993 32814053
Intra
ACOT13 Q9NPJ3 KAT5 Homo sapiens Q92993 32814053
Intra
ACOT13 Q9NPJ3 KAT5 Homo sapiens Q92993 32814053
Intra
ACOT13 Q9NPJ3 SPG21 Homo sapiens Q9NZD8 32296183
Intra
ACOT13 Q9NPJ3 SETDB1 Homo sapiens Q15047-2 32814053
Intra
ACOT13 Q9NPJ3 SETDB1 Homo sapiens Q15047-2 32814053
Intra
ACOT13 Q9NPJ3 SETDB1 Homo sapiens Q15047-2 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant ACOT13 Proteins

Cat. No. Product Name Accession Purity
HY-P7452 ACOT13 Protein, Human (HEK293, His) Q9NPJ3-1 (T2-N140) ≥95%

Related Diseases

Diseases Alias
Dyslexia
Reading Disorder

Specific Reading Disorder

Reading

Dyslexia

Developmental Reading Disorder

Learning Disability

Learning Disabilities

Learning Disorders

Academic Skill Disorder

Learning Disorder

Leukoencephalopathy With Vanishing White Matter

Cree Leukoencephalopathy

Vanishing White Matter Disease

Ovarioleukodystrophy

Vanishing White Matter Leukodystrophy

Childhood Ataxia With Central Nervous System Hypomyelinization

Cach

Cach Syndrome

Myelinosis Centralis Diffusa

VWM

Cle

Childhood Ataxia With Central Nervous System Hypomyelination

Childhood Ataxia With Diffuse Central Nervous System Hypomyelination

Cach/Vwm

Cach/Vwm Syndrome

Childhood Ataxia With Central Nervous System Hypomyelination/Vanishing White Matter

Cree Leukoencehalopathy

Late Infantile Cach Syndrome

Juvenile Or Adult Cach Syndrome

Congenital Or Early Infantile Cach Syndrome

Leukodystrophy With Vanishing White Matter

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 ACOT13 VGNC VGNC:37518
Macaca mulatta ACOT13 VGNC VGNC:69487
Mus musculus ACOT13 MGD MGI:1914084
Bos taurus ACOT13 VGNC VGNC:25549
Felis catus ACOT13 VGNC VGNC:102373
Rattus norvegicus ACOT13 RGD RGD:1306513
Others ACOT13 NCBI