Pgap2
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Official Full Name
PGAP2 post-GPI attachment to proteins 2 [ Homo sapiens ] -
Synonyms
post-GPI attachment to proteins 2;17893;Ensembl:ENSG00000148985;MGC799, FLJ26520;post-GPI attachment to proteins factor 2;FGF receptor activating protein 1;FGF receptor-activating protein 1;cell wall biogenesis 43 N-terminal homolog;FRAG1;CWH43-N
Recombinant Proteins
- Mouse
- Human
- Zebrafish
- Rhesus macaque
- Rat
- Mus musculus
- zebrafish
- Cricetulus griseus
- Xenopus tropicalis (Western clawed frog) (Silurana tropicalis)
- Drosophila melanogaster (Fruit fly)
- Bovine
- Xenopus laevis
- Mammalian Cells
- HEK293
- E.coli
- His
- His&Fc&Avi
Involved Pathway
Pgap2 involved in several pathways and played different roles in them. We selected most pathways Pgap2 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with Pgap2 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|
Protein Function
Pgap2 has several biochemical functions, for example, protein binding,protein transporter activity. Some of the functions are cooperated with other proteins, some of the functions could acted by Pgap2 itself. We selected most functions Pgap2 had, and list some proteins which have the same functions with Pgap2. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| protein transporter activity | SNUPN,RAP1A,KPNB1,AP1S1,TSNAX,AP3S1,SOSTDC1B,TIMM10,COX18,TNPO3 |
| protein binding | UNC119B,SP100,EIF2AK2,ECSIT,NR3C2,SOX1,RBM22,RICTOR,PFTK1,MYO1C |
Interacting Protein
Pgap2 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 Pgap2 here. Most of them are supplied by our site. Hope this information will be useful for your research of Pgap2.
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References
- Horn, D; Wieczorek, D; et al. Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS 22:762-767(2014).
- Ohba, C; Okamoto, N; et al. PIGN mutations cause congenital anomalies, developmental delay, hypotonia, epilepsy, and progressive cerebellar atrophy. NEUROGENETICS 15:85-92(2014).
