ABCB7 Chromosome X
ATP binding cassette subfamily B member 7
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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
RS1057515989
Conflicting classifications of pathogenicity
X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
Health Risk
RS1133577
Conflicting classifications of pathogenicity
Health Risk
RS1133578
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS141119655
Conflicting classifications of pathogenicity
X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
Health Risk
RS143070182
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS151288786
Conflicting classifications of pathogenicity
X-linked sideroblastic anemia with ataxia, Inborn genetic diseases, X-linked sideroblastic anemia with ataxia
Health Risk
RS61323727
Conflicting classifications of pathogenicity
ABCB7-related disorder, Uveal melanoma, Colorectal cancer
Health Risk
RS759437344
Conflicting classifications of pathogenicity
ABCB7-related disorder, Inborn genetic diseases, ABCB7-related disorder
Health Risk
RS766831597
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS952109184
Conflicting classifications of pathogenicity
Health Risk
RS1057518042
Likely pathogenic
X-linked sideroblastic anemia with ataxia, X-linked sideroblastic anemia with ataxia
Health Risk
RS1555945011
Likely pathogenic
Health Risk
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 |