DSCR4
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Official Full Name
Down syndrome critical region gene 4 -
Synonyms
DSCR4;Down syndrome critical region gene 4;3045;ENSG00000184029;DCRB;DSCRB;21q22.2;Down syndrome critical region protein 4;Down syndrome critical region protein 4;Down syndrome critical region protein B
| Cat.# | Product name | Source (Host) | Species | Tag | Protein Length | Price |
|---|---|---|---|---|---|---|
| DSCR4-2885H | Recombinant Human DSCR4 Protein, GST-tagged | Wheat Germ | Human | GST |
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| DSCR4-6809HCL | Recombinant Human DSCR4 293 Cell Lysate | HEK293 | Human | Non |
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| DSCR4-1902H | Recombinant Human DSCR4 Protein, Myc/DDK-tagged, C13 and N15-labeled | HEK293T | Human | Myc&DDK |
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| DSCR4-4199HF | Recombinant Full Length Human DSCR4 Protein, GST-tagged | In Vitro Cell Free System | Human | GST | Full L. 118 amino acids |
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Involved Pathway
DSCR4 involved in several pathways and played different roles in them. We selected most pathways DSCR4 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with DSCR4 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
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Protein Function
DSCR4 has several biochemical functions, for example, molecular_function. Some of the functions are cooperated with other proteins, some of the functions could acted by DSCR4 itself. We selected most functions DSCR4 had, and list some proteins which have the same functions with DSCR4. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| molecular_function | GLTPD2,ORAOV1,TMEM109,MHC2DBB,CLHC1,AMMECR1,PXT1,ITFG3,LMAN1L,MRGPRA7 |
Interacting Protein
DSCR4 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 DSCR4 here. Most of them are supplied by our site. Hope this information will be useful for your research of DSCR4.
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Resources
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References
- Masotti, A; Uva, P; et al. Keppen-Lubinsky Syndrome Is Caused by Mutations in the Inwardly Rectifying K+ Channel Encoded by KCNJ6. AMERICAN JOURNAL OF HUMAN GENETICS 96:295-300(2015).
- Li, Y; Wang, J; et al. Rcan1 Deficiency Impairs Neuronal Migration and Causes Periventricular Heterotopia. JOURNAL OF NEUROSCIENCE 35:610-620(2015).
