
ABCD1 - Wikipedia
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 …
ABCD1 gene: MedlinePlus Genetics
The ABCD1 gene provides instructions for producing the adrenoleukodystrophy protein (ALDP). Learn about this gene and related health conditions.
ABCD1 Gene - GeneCards | ABCD1 Protein | ABCD1 Antibody
Nov 13, 2025 · ABCD1 (ATP Binding Cassette Subfamily D Member 1) is a Protein Coding gene. Diseases associated with ABCD1 include Adrenoleukodystrophy and X-Linked Cerebral …
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 1; ABCD1
Aug 30, 2024 · ABCD1 is a member of the ATP-binding cassette (ABC) transporter superfamily. The superfamily contains membrane proteins that translocate a wide variety of substrates …
ABCD1 | Test catalog | Invitae
Diagnostic testing of this gene is recommended to identify a potential genetic basis for a condition. This type of testing can inform prognosis and clinical care for a symptomatic patient or be used …
ABCD1 ATP binding cassette subfamily D member 1 [Homo …
Jul 5, 2025 · Gene target information for ABCD1 - ATP binding cassette subfamily D member 1 (human). Find diseases associated with this biological target and compounds tested against it …
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 …
GENERAL GUIDELINES POSITIVE RESULTS GUIDE: ABCD1 This document is not part of the Invitae® clini. al report and does not represent medical advice. These are general guidelines …
The ABCD1 Gene: Function and Role in X-ALD Disease
Jul 25, 2025 · Explore the ABCD1 gene’s fundamental role in cellular processes and its profound impact when disrupted, leading to a complex genetic condition.
Structural basis of substrate recognition and translocation by …
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 …