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NIPA1

Official Full Name

non imprinted in Prader-Willi/Angelman syndrome 1
Synonyms

Spg6;

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

Involved Pathway
Protein Function
Interacting Protein
NIPA1 Related Articles

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	MRS2;ADD2;MMGT1;PIP;ADD3;CTNS;ANKH;NIPA1;ANKHA
Transmembrane transport of small molecules	SLC1A7A;SLC39A1;SLC12A5B;SLCO3A1;SLC9A7;SLC17A3;AQP10B;SLC26A3.1;ABCD3B

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	NIPA2;CLDN16;ZDHHC13;NIPAL3;CNNM4;MMGT2;MRS2;NIPA1;NIPAL4

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.

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).