Nipa1 non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human) [ Mus musculus (house mouse) ]
Source: NCBI Gene (ID 233280)
Source: NCBI Gene (ID 233280)
Symbol: Nipa1
Full name: non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)
Gene type: protein coding
RefSeq status: VALIDATED
Organism: Mus musculus
Also known as: 1110027G09Rik; A830014A18Rik; FSP3; Spg6
Summary: Predicted to enable magnesium ion transmembrane transporter activity. Involved in magnesium ion transport. Located in early endosome and plasma membrane. Is expressed in brain. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 6. Orthologous to human NIPA1 (NIPA magnesium transporter 1). [provided by Alliance of Genome Resources, Apr 2022]
Expression: Ubiquitous expression in CNS E18 (RPKM 14.8), cortex adult (RPKM 12.2) and 27 other tissues
Orthologs: human
Gene size: 41117bp
Exon count: 5