NIPA1

  • Official Full Name

    non imprinted in Prader-Willi/Angelman syndrome 1
  • Synonyms

    Spg6
Cat.# Product name Source (Host) Species Tag Protein Length Price
NIPA1-10670M Recombinant Mouse NIPA1 Protein Mammalian Cell Mouse His
NIPA1-1572Z Recombinant Zebrafish NIPA1 Mammalian Cell Zebrafish His
NIPA1-6068M Recombinant Mouse NIPA1 Protein, His (Fc)-Avi-tagged HEK293 Mouse His&Fc&Avi
NIPA1-6068M-B Recombinant Mouse NIPA1 Protein Pre-coupled Magnetic Beads HEK293 Mouse

    Involved Pathway

    NIPA1 involved in several pathways and played different roles in them. We selected most pathways NIPA1 participated on our site, such as Miscellaneous transport and binding events,Transmembrane transport of small molecules, which may be useful for your reference. Also, other proteins which involved in the same pathway with NIPA1 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein
    Miscellaneous transport and binding events ADD1,ADD2,MRS2,ADD3A,EPB49,CTNS,DMTN,AZGP1,MMGT1,MAGT1
    Transmembrane transport of small molecules ABCF1,WNK1,TFA,SLC9A6A,FLVCR1,BEST3,SLC4A3,ABCB8,SLC24A5,SLC2A8

    Protein Function

    NIPA1 has several biochemical functions, for example, magnesium ion transmembrane transporter activity. Some of the functions are cooperated with other proteins, some of the functions could acted by NIPA1 itself. We selected most functions NIPA1 had, and list some proteins which have the same functions with NIPA1. You can find most of the proteins on our site.

    Function Related Protein
    magnesium ion transmembrane transporter activity NIPAL4,ZDHHC17,MAGT1,MMGT2,ZDHHC13,NIPA2,CNNM4,CLDN16,MRS2,NIPAL3

    Interacting Protein

    NIPA1 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with NIPA1 here. Most of them are supplied by our site. Hope this information will be useful for your research of NIPA1.

    Resources

    References

    • Vanlerberghe, C; Petit, F; et al. 15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients. EUROPEAN JOURNAL OF MEDICAL GENETICS 58:140-147(2015).
    • Cox, DM; Butler, MG; et al. The 15q11.2 BP1-BP2 Microdeletion Syndrome: A Review. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 16:4068-4082(2015).

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