NP_001123882.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
NCBI Official Full Name
3-ketoacyl-CoA thiolase, peroxisomal isoform b
NCBI Official Synonym Full Names
acetyl-CoA acyltransferase 1
NCBI Protein Information
3-ketoacyl-CoA thiolase, peroxisomal
UniProt Protein Name
3-ketoacyl-CoA thiolase, peroxisomal
UniProt Synonym Protein Names
Acetyl-CoA acyltransferase; Beta-ketothiolase; Peroxisomal 3-oxoacyl-CoA thiolase
UniProt Synonym Gene Names
UniProt Entry Name
THIK_HUMAN
NCBI Summary for ACAA1
This gene encodes an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of this enzyme leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
UniProt Comments for ACAA1
ACAA1: an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of this enzyme leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Protein type: EC 2.3.1.16; Lipid Metabolism - fatty acid; Acetyltransferase; Amino Acid Metabolism - valine, leucine and isoleucine degradation; Lipid Metabolism - unsaturated fatty acid biosynthesis
Chromosomal Location of Human Ortholog: 3p22.2
Cellular Component: intracellular membrane-bound organelle; membrane; peroxisomal matrix; peroxisome
Molecular Function: acetyl-CoA C-acyltransferase activity; palmitoyl-CoA oxidase activity; protein binding
Biological Process: bile acid metabolic process; cellular lipid metabolic process; fatty acid beta-oxidation; fatty acid beta-oxidation using acyl-CoA oxidase; unsaturated fatty acid metabolic process; very-long-chain fatty acid metabolic process
Disease: D-bifunctional Protein Deficiency
Research Articles on ACAA1
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Products associated with anti-ACAA1 antibody
Pathways associated with anti-ACAA1 antibody
Diseases associated with anti-ACAA1 antibody
Organs/Tissues associated with anti-ACAA1 antibody
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