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

Also Known as FSP3; Spg6; 1110027G09Rik; A830014A18Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 233280

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 References Source
involved in magnesium ion transport IDA
IDA: Inferred from direct assay
17166836 MGI
Cellular Component GO Annotation Evidence References 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

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