Gene Gene information from NCBI Gene database.
Entrez ID 8310
Gene name Acyl-CoA oxidase 3, pristanoyl
Gene symbol ACOX3
Synonyms (NCBI Gene)
-
Chromosome 4
Chromosome location 4p16.1
Summary Acyl-Coenzyme A oxidase 3 also know as pristanoyl -CoA oxidase (ACOX3)is involved in the desaturation of 2-methyl branched fatty acids in peroxisomes. Unlike the rat homolog, the human gene is expressed in very low amounts in liver such that its mRNA was
miRNA miRNA information provided by mirtarbase database.
81
miRTarBase ID miRNA Experiments Reference
MIRT763147 hsa-miR-15a CLIP-seq
MIRT763148 hsa-miR-15b CLIP-seq
MIRT763149 hsa-miR-16 CLIP-seq
MIRT763150 hsa-miR-195 CLIP-seq
MIRT763151 hsa-miR-24 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0003997 Function Acyl-CoA oxidase activity IEA
GO:0005504 Function Fatty acid binding IBA
GO:0005504 Function Fatty acid binding IEA
GO:0005777 Component Peroxisome IBA
GO:0005777 Component Peroxisome IDA 8993592
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603402 121 ENSG00000087008
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O15254
Protein name Peroxisomal acyl-coenzyme A oxidase 3 (EC 1.3.3.6) (Branched-chain acyl-CoA oxidase) (BRCACox) (Pristanoyl-CoA oxidase)
Protein function Oxidizes the CoA-esters of 2-methyl-branched fatty acids.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02770 Acyl-CoA_dh_M 155 266 Acyl-CoA dehydrogenase, middle domain Domain
PF01756 ACOX 510 693 Acyl-CoA oxidase Family
Sequence
MASTVEGGDTALLPEFPRGPLDAYRARASFSWKELALFTEGEGMLRFKKTIFSALENDPL
FARSPGADLSLEKYRELNFLRCKRIFEYDFLSVEDMFKSPLKVPALIQCLGMYDSSLAAK
YLLHSLVFGSAVYSSGSERHLTYIQKIFRMEIFGCFALTELSHGSNTKAIRTTAHYDPAT
EEFIIHSPDFEAAKFWVGNMGKTATHAVVFAKLCVPGDQCHGLHPFIVQIRDPKTLLPMP
GVMVGDIGKKLGQNGLDNGFAMFHKV
RVPRQSLLNRMGDVTPEGTYVSPFKDVRQRFGAS
LGSLSSGRVSIVSLAILNLKLAVAIALRFSATRRQFGPTEEEEIPVLEYPMQQWRLLPYL
AAVYALDHFSKSLFLDLVELQRGLASGDRSARQAELGREIHALASASKPLASWTTQQGIQ
ECREACGGHGYLAMNRLGVLRDDNDPNCTYEGDNNILLQQTSNYLLGLLAHQVHDGACFR
SPLKSVDFLDAYPGILDQKFEVSSVADCLDSAVALAAYKWLVCYLLRETYQKLNQEKRSG
SSDFEARNKCQVSHGRPLALAFVELTVVQRFHEHVHQPSVPPSLRAVLGRLSALYALWSL
SRHAALLYRGGYFSGEQAGEVLESAVLALCSQLKDDAVALVDVIAPPDFVLDSPIGRADG
ELYKNLWGAVLQESKVLERASWWPEFSVNKPVI
GSLKSKL
Sequence length 700
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
16
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs62286003 RCV005901527
Adrenocortical carcinoma, hereditary Benign rs62286003 RCV005901530
Chronic lymphocytic leukemia/small lymphocytic lymphoma Benign rs62286003 RCV005901541
Clear cell carcinoma of kidney Benign rs62286003 RCV005901532
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Inhibit 35335125
Lung Neoplasms Associate 34970420