ABCB7 Chromosome X

ATP binding cassette subfamily B member 7
19 variants 19 Health Risk

Upload your DNA to see your personal genotypes for variants in ABCB7.

What This Gene Does
The membrane-associated 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 MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This gene encodes a half-transporter involved in the transport of heme from the mitochondria to the cytosol. With iron/sulfur cluster precursors as its substrates, this protein may play a role in metal homeostasis. Mutations in this gene have been associated with mitochondrial iron accumulation and isodicentric (X)(q13) and sideroblastic anemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2012]
Gene Info
Gene Group
ATP binding cassette subfamily B
Locus Type
gene with protein product
Location
Xq13.3
Ensembl
ENSG00000131269
Associated Conditions (30)
X-linked sideroblastic anemia with ataxia
Inborn genetic diseases
ABCB7-related disorder
Uveal melanoma
Colorectal cancer
Thymoma
Melanoma
Lung cancer
Ovarian cancer
Clear cell carcinoma of kidney
Colon adenocarcinoma
Thyroid cancer
nonmedullary
1
Cholangiocarcinoma
Cervical cancer
Uterine corpus endometrial carcinoma
Chronic lymphocytic leukemia/small lymphocytic lymphoma
Acute myeloid leukemia
Hepatocellular carcinoma
+10 more conditions
Key Variants
All Variants (19)
RSID Category Clinical Significance Conditions
RS1057515989 Health Risk Conflicting classifications of pathogenicity X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
RS1133577 Health Risk Conflicting classifications of pathogenicity
RS1133578 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS141119655 Health Risk Conflicting classifications of pathogenicity X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
RS143070182 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS151288786 Health Risk Conflicting classifications of pathogenicity X-linked sideroblastic anemia with ataxia, Inborn genetic diseases, X-linked sideroblastic anemia with ataxia
RS61323727 Health Risk Conflicting classifications of pathogenicity ABCB7-related disorder, Uveal melanoma, Colorectal cancer
RS759437344 Health Risk Conflicting classifications of pathogenicity ABCB7-related disorder, Inborn genetic diseases, ABCB7-related disorder
RS766831597 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS952109184 Health Risk Conflicting classifications of pathogenicity
RS1057518042 Health Risk Likely pathogenic X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
RS1555945011 Health Risk Likely pathogenic
RS2519831064 Health Risk Likely pathogenic
RS762876355 Health Risk Likely pathogenic X-linked sideroblastic anemia with ataxia, Nonpapillary renal cell carcinoma, X-linked sideroblastic anemia with ataxia
RS797044558 Health Risk Likely pathogenic Spinocerebellar ataxia, X-linked, Inborn genetic diseases
RS80356713 Health Risk Likely pathogenic X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
RS515726147 Health Risk Pathogenic X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
RS72554634 Health Risk Pathogenic X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
RS80356714 Health Risk Pathogenic X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
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