Reference for ACOX1. Search for ACOX1

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ACOX1

ACOX1

Protein-coding gene in the species Homo sapiens

acyl-coenzyme A oxidase 1 is an enzyme that in humans is encoded by the ACOX1 gene. The protein encoded by this gene is the first enzyme of the fatty

ACOX1

Acyl-CoA oxidase deficiency

Medical condition

pathogenic variants in ACOX1, which codes for the production of an enzyme called peroxisomal straight-chain acyl-CoA oxidase (ACOX1). It is responsible for

Acyl-CoA oxidase deficiency

Acyl-CoA_oxidase_deficiency

Peroxisome proliferator-activated receptor alpha

Nuclear receptor protein found in humans

number in the hundreds. Classical target genes of PPAR-alpha include PDK4, ACOX1, and CPT1. Low and high throughput gene expression analysis have allowed

Peroxisome proliferator-activated receptor alpha

Peroxisome_proliferator-activated_receptor_alpha

Tellimagrandin I

Chemical compound

acid beta-oxidation in liver, increasing mRNA expression of PPAR alpha, ACOX1, and CPT1A. It enhances gap junction communication and reduces tumor phenotype

Tellimagrandin I

Tellimagrandin_I

List of human protein-coding genes 1

Q8WXI4 169 ACOT12 HGNC:24436; Q8WYK0 170 ACOT13 HGNC:20999; Q9NPJ3 171 ACOX1 HGNC:119; Q15067 172 ACOX2 HGNC:120; Q99424 173 ACOX3 HGNC:121; O15254 174

List of human protein-coding genes 1

List_of_human_protein-coding_genes_1

Peroxisomal disorder

Medical condition

Hyperoxaluria type 1 259900 AGXT E80.311 Acyl-CoA oxidase deficiency 264470 ACOX1 E80.313 D-bifunctional protein deficiency 261515 HSD17B4 E80.314 Dihydroxyacetonephosphate

Peroxisomal disorder

Peroxisomal_disorder

Acox

Surname list

and jazz drummer Kristófer Acox (born 1993), Icelandic basketball player ACOX1, human gene which encodes the enzyme peroxisomal acyl-coenzyme A oxidase

Acox

ACOX3

Protein-coding gene in the species Homo sapiens

in a tissue specific manner in tissues that have not yet been examined. ACOX1 Acyl-CoA oxidase GRCh38: Ensembl release 89: ENSG00000087008 – Ensembl,

ACOX3

Retinoid X receptor alpha

Protein-coding gene in the species Homo sapiens

for PPARA transcriptional activity on fatty acid oxidation genes such as ACOX1 and the cytochrome P450 system genes. Click on genes, proteins and metabolites

Retinoid X receptor alpha

Retinoid_X_receptor_alpha

Acyl-CoA oxidase

InterPro Family

enzymes, with PDB accession codes 1IS2, 1W07, 2DDH, 2FON, 2IX5, and 2IX6. ACOX1 ACOX3 Kawaguchi A, Tsubotani S, Seyama Y, et al. (November 1980). "Stereochemistry

Acyl-CoA oxidase

Acyl-CoA_oxidase

HSD17B4

Protein-coding gene in the species Homo sapiens

de Duve (1976), is catalyzed by 3 enzymes: acyl-CoA oxidase (see, e.g., ACOX1, MIM 609751); the 'D-bifunctional enzyme,' with enoyl-CoA hydratase and

HSD17B4

MINDY1

Protein-coding gene in the species Homo sapiens

following genes have interactions with FAM63A: GSPT2, NAA38, RNMT, CSNIK1G2, ACOX1, PSMC1, SLC25A37, MMS19, DIAPH1, ME1, GAPDH, UBC. After performing a yeast

MINDY1

List of OMIM disorder codes

microcephaly; 608097; ARFGEF2 Peroxisomal acyl-CoA oxidase deficiency; 264470; ACOX1 Perry syndrome; 168605; DCTN1 Persistent Müllerian duct syndrome, type I;

List of OMIM disorder codes

List_of_OMIM_disorder_codes