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SH3TC2

  • Official Full Name

    SH3 domain and tetratricopeptide repeats 2

  • Overview

    This gene encodes a protein with two N-terminal Src homology 3 (SH3) domains and 10 tetratricopeptide repeat (TPR) motifs, and is a member of a small gene family. The gene product has been proposed to be an adapter or docking molecule. Mutations in this gene result in autosomal recessive Charcot-Marie-Tooth disease type 4C, a childhood-onset neurodegenerative disease characterized by demyelination of motor and sensory neurons.
  • Synonyms

    SH3TC2; SH3 domain and tetratricopeptide repeats 2; SH3 domain and tetratricopeptide repeat-containing protein 2; CMT4C; KIAA1985; SH3 domain and tetratricopeptide repeats-containing protein 2; MNMN; FLJ13605;
Species Cat.# Product name Source (Host) Tag Protein Length Price
Human SH3TC2-3273H Recombinant Human SH3TC2 protein, His-tagged E.coli His
  • SH3TC2 Related Articles

SH3TC2 involved in several pathways and played different roles in them. We selected most pathways SH3TC2 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with SH3TC2 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein

SH3TC2 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by SH3TC2 itself. We selected most functions SH3TC2 had, and list some proteins which have the same functions with SH3TC2. You can find most of the proteins on our site.

Function Related Protein

SH3TC2 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 SH3TC2 here. Most of them are supplied by our site. Hope this information will be useful for your research of SH3TC2.

Zimon, M; Battaloglu, E; et al. Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach. NEUROGENETICS 16:33-42(2015).
Brewer, MH; Ma, KH; et al. Haplotype-specific modulation of a SOX10/CREB response element at the Charcot Marie Tooth disease type 4C locus SH3TC2. HUMAN MOLECULAR GENETICS 23:5171-5187(2014).
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