ABCD4 Chromosome 14

ATP binding cassette subfamily D member 4
33 variants 33 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. The function of this peroxisomal membrane protein is unknown. However, it is speculated that it may function as a heterodimer for another peroxisomal ABC transporter and, therefore, may modify the adrenoleukodystrophy phenotype. It may also play a role in the process of peroxisome biogenesis. Alternative splicing results in several protein-coding and non-protein-coding variants. [provided by RefSeq, Jul 2017]
Gene Info
Gene Group
ATP binding cassette subfamily D
Locus Type
gene with protein product
Location
14q24.3
Ensembl
ENSG00000119688
Associated Conditions (7)
Methylmalonic acidemia with homocystinuria
type cblJ
Inborn genetic diseases
ABCD4-related disorder
Malignant tumor of urinary bladder
Cobalamin C disease
Familial cancer of breast
Key Variants
RS139901585
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Inborn genetic diseases
Health Risk
RS1410990711
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
Health Risk
RS141868117
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, ABCD4-related disorder
Health Risk
RS142696207
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Inborn genetic diseases
Health Risk
RS147446660
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Inborn genetic diseases
Health Risk
RS151116417
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Malignant tumor of urinary bladder
Health Risk
RS200761248
Conflicting classifications of pathogenicity
Inborn genetic diseases, Methylmalonic acidemia with homocystinuria, type cblJ
Health Risk
RS201777056
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Cobalamin C disease
Health Risk
RS45568335
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, ABCD4-related disorder
Health Risk
RS763777109
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
Health Risk
RS765378243
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
Health Risk
RS930102975
Conflicting classifications of pathogenicity
Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
Health Risk
All Variants (33)
RSID Category Clinical Significance Conditions
RS139901585 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Inborn genetic diseases
RS1410990711 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS141868117 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, ABCD4-related disorder
RS142696207 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Inborn genetic diseases
RS147446660 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Inborn genetic diseases
RS151116417 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Malignant tumor of urinary bladder
RS200761248 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Methylmalonic acidemia with homocystinuria, type cblJ
RS201777056 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Cobalamin C disease
RS45568335 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, ABCD4-related disorder
RS763777109 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS765378243 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS930102975 Health Risk Conflicting classifications of pathogenicity Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS1390206641 Health Risk Likely pathogenic Cobalamin C disease, Cobalamin C disease
RS1408519111 Health Risk Likely pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS142443294 Health Risk Likely pathogenic Cobalamin C disease, Familial cancer of breast, Cobalamin C disease
RS2082518811 Health Risk Likely pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS2505794258 Health Risk Likely pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS745414252 Health Risk Likely pathogenic Cobalamin C disease, Methylmalonic acidemia with homocystinuria, type cblJ
RS1159673131 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS1282760239 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS1435760575 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS1440898011 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS2080853826 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS2505238680 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS2505333886 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS2505338898 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS2505983851 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS387907315 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS769298254 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS769364566 Health Risk Pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Methylmalonic acidemia with homocystinuria
RS780512428 Health Risk Pathogenic Cobalamin C disease, Cobalamin C disease
RS767795583 Health Risk Pathogenic/Likely pathogenic Methylmalonic acidemia with homocystinuria, type cblJ, Cobalamin C disease
RS776529140 Health Risk Pathogenic/Likely pathogenic Cobalamin C disease, Methylmalonic acidemia with homocystinuria, type cblJ
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