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DSCR4

  • 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;
Species Cat.# Product name Source (Host) Tag Protein Length Price
Human DSCR4-2885H Recombinant Human DSCR4 Protein, GST-tagged Wheat Germ GST
Human DSCR4-6809HCL Recombinant Human DSCR4 293 Cell Lysate HEK293 N/A
Human DSCR4-4199HF Recombinant Full Length Human DSCR4 Protein, GST-tagged In Vitro Cell Free System GST 118 amino acids
Human DSCR4-1902H Recombinant Human DSCR4 Protein, Myc/DDK-tagged, C13 and N15-labeled HEK293T Myc/DDK
  • Involved Pathway
  • Protein Function
  • Interacting Protein
  • DSCR4 Related Articles

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

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_functionTMEM239;ANKRD13A;CAPN6;PLEKHD1;FMNL1;FAM69B;TVP23B;TAS2R109;DSCR9

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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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).
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