2. Gene
  3. Nipa1 - non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human) Gene

Nipa1 - non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human) Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Mus musculus

Also known as FSP3; Spg6; 1110027G09Rik; A830014A18Rik

Gene ID: 233280 | Gene type: protein coding

About Nipa1

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]

Nipa1 Products(1)

mRNA Protein Name
NM_153578.3 NP_705806.1 magnesium transporter NIPA1
Gene Ontology
  • Biological Process
  • Cellular Component
Biological Process GO Annotation Evidence Reference Source
involved in magnesium ion transport IDA
IDA: Inferred from direct assay
17166836 MGI
Cellular Component GO Annotation Evidence Reference Source
located in early endosome IDA
IDA: Inferred from direct assay
17166836 MGI
located in plasma membrane IDA
IDA: Inferred from direct assay
17166836 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

magnesium transporter NIPA1

non-imprinted in Prader-Willi/Angelman syndrome region protein 1 homolog

spastic paraplegia 6 homolog

Related Agents

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