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DFNB59

Official Full Name

deafness, autosomal recessive 59
Overview

The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59).
Synonyms

DFNB59; deafness, autosomal recessive 59; pejvakin; autosomal recessive deafness type 59 protein; PJVK;

Species	Cat.#	Product name	Source (Host)	Tag	Price
Human	DFNB59-977H	Recombinant Human DFNB59	Mammalian Cell	His	Inquiry
Human	DFNB59-2794H	Recombinant Human DFNB59 Protein, His (Fc)-Avi-tagged	HEK293	His (Fc)-Avi	Inquiry
Human	DFNB59-2794H-B	Recombinant Human DFNB59 Protein Pre-coupled Magnetic Beads	HEK293		Inquiry

DFNB59 Related Articles

DFNB59 involved in several pathways and played different roles in them. We selected most pathways DFNB59 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with DFNB59 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name	Pathway Related Protein

DFNB59 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by DFNB59 itself. We selected most functions DFNB59 had, and list some proteins which have the same functions with DFNB59. You can find most of the proteins on our site.

Function	Related Protein

DFNB59 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 DFNB59 here. Most of them are supplied by our site. Hope this information will be useful for your research of DFNB59.

Zhao, JD; Yuan, YY; et al. KCNJ10 May Not Be a Contributor to Nonsyndromic Enlargement of Vestibular Aqueduct (NSEVA) in Chinese Subjects. PLOS ONE 9:-(2014).

Tamayo, ML; Olarte, M; et al. Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogota, Colombia: Results of a screening program. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY 73:97-101(2009).