SH3TC2 Polyclonal Antibody, 50ul Bio-Reaction Tube Mutations in this gene result

Mutations in this gene result in autosomal dominant hereditary thrombophilia

or protein kinase C activation

This gene encodes a DNA-binding protein which has high specificity for scaffold or matrix attachment region DNA elements (S/MAR DNA)

|subunit:Interacts with HIV-1 Tat

disease:Defects in OSMR are the cause of amyloidosis type 9 (AMYL9)

SH3TC2 Polyclonal Antibody, 50ul Bio-Reaction Tube Mutations in this gene resultSH3TC2 (SH3 domain and tetratricopeptide repeats 2) 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