XB-FEAT-961418: Difference between revisions
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=nipa1= | =nipa1= | ||
This is the community wiki page for the gene ''nipa1'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''nipa1'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | ||
=summary from NCBI= | |||
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] | |||
=nomenclature changes= | |||
03.12.18 | |||
Human name has changed for Entrez Gene: 123606. From non imprinted in Prader-Willi/Angelman syndrome 1 to NIPA magnesium transporter 1 | |||
Latest revision as of 13:03, 13 March 2018
nipa1
This is the community wiki page for the gene nipa1 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
summary from NCBI
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]
nomenclature changes
03.12.18 Human name has changed for Entrez Gene: 123606. From non imprinted in Prader-Willi/Angelman syndrome 1 to NIPA magnesium transporter 1