ABCD1 is a protein that transfers fatty acids into peroxisomes. The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins …

Mar 28, 2025 · ABCD1 (ATP Binding Cassette Subfamily D Member 1) is a Protein Coding gene. Diseases associated with ABCD1 include Adrenoleukodystrophy and …

ABCD1 contains 10 exons and is located on the long arm of the X chromosome. It encodes for the ATP-binding cassette (ABC) subfamily D member 1 protein, a peroxisomal membrane …

Mar 26, 1999 · ABCD1 encodes adrenoleukodystrophy protein (ALDP), a member of the ATP-binding cassette (ABC) protein transporter family. This protein serves as a transporter of …

The ABCD1 gene provides instructions for producing the adrenoleukodystrophy protein (ALDP). Learn about this gene and related health conditions.

The progressive neurometabolic disorder X-linked adrenoleukodystrophy (ALD) is caused by pathogenic variants in the ABCD1 gene, which encodes the peroxisomal ATP-binding …

Feb 8, 2025 · ABCD1 mutation in the ethiopathogenesis of X-linked adrenoleukodystrophy. Its defect causes accumulation of the very long chain fatty acids in the tissues of the central and …

Jun 8, 2022 · Human ABC transporter ABCD1 transports very long-chain fatty acids from cytosol to peroxisome for β-oxidation, dysfunction of which usually causes the X-linked …

The ABCD1 gene encodes the Adrenoleukodystrophy protein. Defects in this gene result in abnormal peroxisomal beta-oxidation, causing accumulation of very long chain fatty acids …

Aug 30, 2024 · ABCD1 (ALDP) maps to Xq28 and is mutated in the X-linked disorder adrenoleukodystrophy (ALD; 300100). ABCD1 is a member of the ATP-binding cassette (ABC) …