Homo sapiens Protein: NIPA2
Summary
InnateDB Protein IDBP-583125.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NIPA2
Protein Name non imprinted in Prader-Willi/Angelman syndrome 2
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000437746
InnateDB Gene IDBG-3989 (NIPA2)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0015095 magnesium ion transmembrane transporter activity
Biological Process
GO:0015693 magnesium ion transport
Cellular Component
GO:0005769 early endosome
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR000620 Drug/metabolite transporter
IPR008521 Magnesium transporter NIPA
PFAM PF00892
PF05653
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8N8Q9
PhosphoSite PhosphoSite-Q8N8Q9
TrEMBL
UniProt Splice Variant
Entrez Gene 81614
UniGene
RefSeq NP_001008894
HUGO HGNC:17044
OMIM 608146
CCDS CCDS73694
HPRD 16290
IMGT
EMBL AC011767 AK096305 AK300843 AY732242 BC000957 BC011775 BK001120 CR606982
GenPept AAH00957 AAH11775 AAU34000 BAC04757 BAG62494 DAA01509