1. Gene
  2. Nipa2 - non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human) Gene

Nipa2 - non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human) Gene

Mus musculus

Also known as 2600017P10Rik; 3830408P04Rik

Gene ID: 93790 | Gene type: protein coding

About Nipa2

Summary

Predicted to enable magnesium ion transmembrane transporter activity. Involved in magnesium ion transport. Located in early endosome and plasma membrane. Orthologous to human NIPA2 (NIPA magnesium transporter 2). [provided by Alliance of Genome Resources, Apr 2022]

Nipa2 Products(5)

mRNA Protein Name
NM_001256130.1 NP_001243059.1 magnesium transporter NIPA2 isoform 1
NM_001256131.1 NP_001243060.1 magnesium transporter NIPA2 isoform 1
NM_001256132.1 NP_001243061.1 magnesium transporter NIPA2 isoform 1
NM_001256133.1 NP_001243062.1 magnesium transporter NIPA2 isoform 2
NM_023647.6 NP_076136.2 magnesium transporter NIPA2 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
11591653 MGI
Biological Process GO Annotation Evidence Reference Source
involved in magnesium ion transport IDA
IDA: Inferred from direct assay
18667602 MGI
Cellular Component GO Annotation Evidence Reference Source
located in early endosome IDA
IDA: Inferred from direct assay
18667602 MGI
located in plasma membrane IDA
IDA: Inferred from direct assay
18667602 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 NIPA2

non-imprinted in Prader-Willi/Angelman syndrome region protein 2 homolog

Orthologs Information

Species Symbol Source ID
Homo sapiens Nipa2 NCBI NCBI:81614