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WBSCR16

Official Full Name

Williams-Beuren syndrome chromosome region 16
Overview

This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Synonyms

WBSCR16; Williams-Beuren syndrome chromosome region 16; Williams-Beuren syndrome chromosomal region 16 protein; 5730496C04Rik; MGC44931; AU019812; DKFZp434D0421; MGC189739; RCC1-like G exchanging factor-like protein; WBS16_HUMAN;

Species	Cat.#	Product name	Source (Host)	Tag	Price
Human	WBSCR16-1921HCL	Recombinant Human WBSCR16 cell lysate		N/A	Inquiry
Zebrafish	WBSCR16-5213Z	Recombinant Zebrafish WBSCR16	Mammalian Cell	His	Inquiry
Chicken	WBSCR16-1361C	Recombinant Chicken WBSCR16	Mammalian Cell	His	Inquiry

WBSCR16 Related Articles

WBSCR16 involved in several pathways and played different roles in them. We selected most pathways WBSCR16 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with WBSCR16 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name	Pathway Related Protein

WBSCR16 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by WBSCR16 itself. We selected most functions WBSCR16 had, and list some proteins which have the same functions with WBSCR16. You can find most of the proteins on our site.

Function	Related Protein

WBSCR16 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 WBSCR16 here. Most of them are supplied by our site. Hope this information will be useful for your research of WBSCR16.

Frohnauer, J; Caliebe, A; et al. No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control. MOLECULAR CYTOGENETICS 3:-(2010).

Bosch, N; Morell, M; et al. Nucleotide, Cytogenetic and Expression Impact of the Human Chromosome 8p23.1 Inversion Polymorphism. PLOS ONE 4:-(2009).