NIPA1
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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.
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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).