Text Size:AAA

ABCB7  Protein

All ABCB7 Reagents

Browse ABCB7 Products by

ABCB7 Related Pathways

ABCB7 Related Protein, Antibody, cDNA Gene, and ELISA Kits

ABCB7 Related Protein, Antibody, cDNA Gene, and ELISA Kits

Featured Reagent Products

ABCB7 Summary & Protein Information

ABCB7 Background

Subunit structure: Homodimer or heterodimer (Potential).
Subcellular location: Mitochondrion inner membrane; Multi-pass membrane protein (Potential).
Involvement in disease: Anemia, sideroblastic, spinocerebellar ataxia (ASAT) [MIM:301310]: A X-linked recessive disorder characterized by an infantile to early childhood onset of non-progressive cerebellar ataxia and mild anemia, with hypochromia and microcytosis. Note=The disease is caused by mutations affecting the gene represented in this entry.
Sequence similarity: Belongs to the ABC transporter superfamily. ABCB family. Heavy Metal importer (TC 3.A.1.210) subfamily.
Contains 1 ABC transmembrane type-1 domain.
Contains 1 ABC transporter domain.
General information above from UniProt

ABCB7 Alternative Name

ABC7,ASAT,Atm1p,EST140535, [homo-sapiens]
Abc7,AA517758,AU019072, [mus-musculus]

ABCB7 Related Studies

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"