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ABCB7

Protein-coding gene in humans From Wikipedia, the free encyclopedia

ABCB7
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ATP-binding cassette sub-family B member 7, mitochondrial is a protein that in humans is encoded by the ABCB7 gene.[5][6]

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Function

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.

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Clinical significance

Mutations in this gene have been implicated in X-linked sideroblastic anemia with ataxia.[6]

Interactions

ABCB7 has been shown to interact with Ferrochelatase.[7]

See also

References

Further reading

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