ABCD3 Chromosome 1

ATP binding cassette subfamily D member 3
1 variant 1 Health Risk

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What This Gene Does
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"ATP binding cassette subfamily D|GOLD domain containing"
Locus Type
gene with protein product
Location
1p21.3
Ensembl
ENSG00000117528
Associated Conditions (3)
Uterine corpus endometrial carcinoma
Cervical cancer
Clear cell carcinoma of kidney
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS75418934 Health Risk Conflicting classifications of pathogenicity Uterine corpus endometrial carcinoma, Cervical cancer, Clear cell carcinoma of kidney
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