NIPA2

NIPA2
Identifiers
Aliases	NIPA2, non imprinted in Prader-Willi/Angelman syndrome 2, SLC57A2, NIPA magnesium transporter 2
External IDs	OMIM: 608146; MGI: 1913918; HomoloGene: 11368; GeneCards: NIPA2; OMA:NIPA2 - orthologs
Gene location (Human)
Chr.	Chromosome 15 (human)
End	22,869,362 bp
Gene location (Mouse)
Chr.	Chromosome 7 (mouse)
End	55,612,224 bp
RNA expression pattern
	Top expressed in
	pancreatic ductal cell; ; mucosa of colon; ; mucosa of sigmoid colon; ; secondary oocyte; ; mucosa of ileum; ; nasal epithelium; ; rectum; ; right ventricle; ; islet of Langerhans; ; duodenum;
	Top expressed in
	epithelium of small intestine; ; submandibular gland; ; gastrula; ; ileum; ; left colon; ; transitional epithelium of urinary bladder; ; interventricular septum; ; atrioventricular valve; ; jejunum; ; epithelium of stomach;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	magnesium ion transmembrane transporter activity;
Cellular component	integral component of membrane; endosome; plasma membrane; early endosome; membrane;
Biological process	magnesium ion transmembrane transport; ion transport; magnesium ion transport;
	Sources:Amigo / QuickGO
Orthologs
	81614
	93790
	ENSG00000140157
	ENSMUSG00000030452
	Q8N8Q9
	Q9JJC8
NM_001008860; NM_001008892; NM_001008894; NM_001184888; NM_001184889;
	NM_030922
	NM_001256130; NM_001256131; NM_001256132; NM_001256133; NM_023647
NP_001008860; NP_001008892; NP_001008894; NP_001171817; NP_001171818;
	NP_112184
	NP_001243059; NP_001243060; NP_001243061; NP_001243062; NP_076136
	Wikidata
View/Edit Human	View/Edit Mouse

Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 is a protein that in humans is encoded by the NIPA2 gene.