NIPA1( Human )

Entrez Gene 123606 Entrez Gene 123606
non imprinted in Prader-Willi/Angelman syndrome 1

Alias

FSP3|SPG6

This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008].

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