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ACADVL

ACADVL

Protein-coding gene in the species Homo sapiens

mitochondrial (VLCAD) is an enzyme that in humans is encoded by the ACADVL gene. Mutations in the ACADVL are associated with very long-chain acyl-coenzyme A dehydrogenase

ACADVL

Very long chain fatty acid

Fatty acid with 22 or more carbons

lumequeic acid (Δ21-30:1). The edge case wax acid is behenic acid (C-22). ACADVL SLC27A2 SLC27A5 Cerotic acid, the fatty acid associated with adrenoleukodystrophy

Very long chain fatty acid

Very_long_chain_fatty_acid

Chromosome 17

Human chromosome

Ubiquitin carboxyl-terminal hydrolase 6 linked to Aneurysmal bone cyst (17p13) ACADVL: acyl-coenzyme A dehydrogenase, very long chain (17p13.1) SHBG: Sex hormone

Chromosome 17

Chromosome_17

Very-long-chain acyl-CoA dehydrogenase

Very-long-chain acyl-CoA dehydrogenase (EC 1.3.8.9, ACADVL (gene).) is an enzyme with systematic name very-long-chain acyl-CoA:electron-transfer flavoprotein

Very-long-chain acyl-CoA dehydrogenase

Very-long-chain_acyl-CoA_dehydrogenase

ACAD9

Protein-coding gene in the species Homo sapiens

56–38% similarity with the eight members of the ACAD family, including ACADVL, ACADS, ACADM, ACADL, IVD, GCD, ACADSB, and ACD8. The calculated molecular

ACAD9

List of human protein-coding genes 1

HGNC:89; P11310 127 ACADS HGNC:90; P16219 128 ACADSB HGNC:91; P45954 129 ACADVL HGNC:92; P49748 130 ACAN HGNC:319; P16112 131 ACAP1 HGNC:16467; Q15027 132

List of human protein-coding genes 1

List_of_human_protein-coding_genes_1

Very long-chain acyl-coenzyme A dehydrogenase deficiency

Medical condition

body, giving rise to the array of symptoms listed above. Mutations in the ACADVL gene lead to inadequate levels of an enzyme called very long-chain acyl-coenzyme

Very long-chain acyl-coenzyme A dehydrogenase deficiency

Very_long-chain_acyl-coenzyme_A_dehydrogenase_deficiency

FASTKD3

Protein-coding gene in the species Homo sapiens

to interact with: FASTKD2; Fatty acid beta oxidation pathway proteins (ACADVL, ECHS1, HADHA, HADHB, ACAA2); Amino acid catabolic pathways proteins (MCCC1

FASTKD3

List of OMIM disorder codes

BEST1 Vitreoretinochoroidopathy; 193220; BEST1 VLCAD deficiency; 201475; ACADVL Vohwinkel syndrome with ichthyosis; 604117; LOR Vohwinkel syndrome; 124500;

List of OMIM disorder codes

List_of_OMIM_disorder_codes