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Description for Protein NIPA2

non imprinted in Prader-Willi/Angelman syndrome 2
No Interacting Proteins
Icon Book Platelet Evidence (proteome studies/others : 0/1)
(platelet: 1)
Summary:
This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21. (PubMed Links)
Domains and Motifs:
  • TM: Transmembrane domain
    • Gene Ontology:
    Gene Ontology Annotations
    KEGG - Enzyme ID(s):
    None Available
    KEGG - Orthology:
    None Available
    KEGG - Pathway(s):
    None Available
    Nomenclature / Alternative Names:
    Non imprinted in Prader-Willi/Angelman syndrome 2 isoform a; non imprinted in Prader-Willi/Angelman syndrome 2 isoform b; Non imprinted in Prader-Willi/Angelman syndrome 2; MGC5466
    Approved Symbol:
    NIPA2
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 2
    Human (de-) phosphorylation sites: 2; No platelet phosphorylation sites
    Phosphorylation Targets:
    Total phosphorylation targets: 0
    Human phosphorylation targets: 0;Predicted platelet targets: 0
    		Protein Characteristics:
    Isoform-specific Information
    Icon DrugsAssociated Drugs (DrugBank Accession):

    None Available

    Associated Genetic Diseases:

    None Available
    		Predicted Transmembrane Domains:
  • Isoform 4 : 7
  • Isoform 3 : 9
  • Isoform 2 : 9
  • Isoform 1 : 9
    • Additional Identifiers:

    HPRD: 16290 Entrez Gene ID: 81614 OMIM ID: 608146 Swissprot Accession: Q8N8Q9; A6NFH4;