ACAA1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

3-Ketoacyl-CoA thiolase, peroxisomal also known as acetyl-Coenzyme A acyltransferase 1 is an enzyme that in humans is encoded by the ACAA1 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesACAA1, ACAA, PTHIO, THIO, acetyl-CoA acyltransferase 1, Lnc-Myd88
Quick facts Available structures, PDB ...
ACAA1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesACAA1, ACAA, PTHIO, THIO, acetyl-CoA acyltransferase 1, Lnc-Myd88
External IDsOMIM: 604054; MGI: 2148491; HomoloGene: 37497; GeneCards: ACAA1; OMA:ACAA1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001130410
NM_001607

NM_130864
NM_001357516

RefSeq (protein)

NP_001123882
NP_001598
NP_001598.1

NP_570934
NP_001344445

Location (UCSC)Chr 3: 38.1 – 38.14 MbChr 9: 119.17 – 119.18 Mb
PubMed search[3][4]
Wikidata
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Acetyl-Coenzyme A acyltransferase 1 is an acetyl-CoA C-acyltransferase enzyme.

Function

This gene encodes an enzyme operative in the beta oxidation system of the peroxisomes.[5]

Clinical significance

Deficiency of this enzyme leads to pseudo-Zellweger syndrome.[5]

References

Further reading

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