Nipa1 - NIPA magnesium transporter 1 Gene

Also Known as Spg6; SLC56A1

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 308668

Summary

Predicted to enable magnesium ion transmembrane transporter activity. Predicted to be involved in magnesium ion transport. Predicted to be located in early endosome and plasma membrane. 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]

Nipa1 Products (1)

mRNA Protein Name
NM_001107519.1 NP_001100989.1 magnesium transporter NIPA1
Protein Preferred Names Protein Names

magnesium transporter NIPA1

  • non imprinted in Prader-Willi/Angelman syndrome 1 homolog

  • solute carrier family 56 member 1

  • spastic paraplegia 6 (autosomal dominant)

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS09302 NIPA1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Nipa1 NCBI NCBI:123606