-
mitochondrial (VLCAD) is an
enzyme that in
humans is
encoded by the
ACADVL gene.
Mutations in the
ACADVL are ****ociated with very long-chain acyl-coenzyme A dehydrogenase...
- acid (Δ15-24:1),
ximenic acid (Δ17-26:1), and
lumequeic acid (Δ21-30:1).
ACADVL SLC27A2 SLC27A5
Cerotic acid, the
fatty acid ****ociated with adrenoleukodystrophy...
-
ACADM 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...
-
Ubiquitin carboxyl-terminal
hydrolase 6
linked to
Aneurysmal bone cyst (17p13)
ACADVL: acyl-coenzyme A dehydrogenase, very long
chain (17p13.1) SHBG: **** hormone...
- 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-CoA
dehydrogenase (EC 1.3.8.9,
ACADVL (gene).) is an
enzyme with
systematic name very-long-chain acyl-CoA:electron-transfer flavoprotein...
- 56–38%
similarity with the
eight members of the ACAD family,
including ACADVL, ACADS, ACADM, ACADL, IVD, GCD, ACADSB, and ACD8. The
calculated molecular...
- to
interact with: FASTKD2;
Fatty acid beta
oxidation pathway proteins (
ACADVL, ECHS1, HADHA, HADHB, ACAA2);
Amino acid
catabolic pathways proteins (MCCC1...
- BEST1 Vitreoretinochoroidopathy; 193220; BEST1
VLCAD deficiency; 201475;
ACADVL Vohwinkel syndrome with ichthyosis; 604117; LOR
Vohwinkel syndrome; 124500;...
