RecName: Full=Metal cation symporter ZIP14; AltName: Full=LIV-1 subfam - Protein

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Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in SLC39A14 Mutation Carriers and Genetic Animal Models. [Int J Mol Sci. 2022]
Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in SLC39A14 Mutation Carriers and Genetic Animal Models.
Rodichkin AN, Guilarte TR. Int J Mol Sci. 2022 Oct 24; 23(21). Epub 2022 Oct 24.
Benign SLC39A14 Course of Dystonia-Parkinsonism Secondary to Inherited Manganese Accumulation. [Mov Disord Clin Pract. 2020]
Benign SLC39A14 Course of Dystonia-Parkinsonism Secondary to Inherited Manganese Accumulation.
Namnah M, Bauer M, Mor-Shaked H, Bressman SB, Raymond D, Ozelius LJ, Arkadir D. Mov Disord Clin Pract. 2020 Jul; 7(5):569-570. Epub 2020 May 7.
Autosomal-recessive iron deficiency anemia, dystonia and hypermanganesemia caused by new variant mutation of the manganese transporter gene SLC39A14. [Acta Neurol Belg. 2019]
Autosomal-recessive iron deficiency anemia, dystonia and hypermanganesemia caused by new variant mutation of the manganese transporter gene SLC39A14.
Zeglam A, Abugrara A, Kabuka M. Acta Neurol Belg. 2019 Sep; 119(3):379-384. Epub 2018 Sep 19.

RefSeq genomic sequence
See the genomic reference sequence for the SLC39A14 gene (NG_054890.1).
RefSeq protein isoforms
See 18 reference sequence protein isoforms for the SLC39A14 gene.

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Q15043 [Domain Mapping of Disease Mut...]
Q15043
Domain Mapping of Disease Mutations
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Protein