STX16 Rabbit Polyclonal Antibody, 100ul Electrophoresis & Labeling Mutations in this gene result

Mutations in this gene result in congenital disorder of glycosylation type If

Diseases associated with GBP5 include chronic active epstein-barr virus infection

among other targets

which always presents with retinal degeneration (SCA7)

Involved in the regulation of neuronal migration through its dual activities in regulating cellular polarity and microtubule dynamics

STX16 Rabbit Polyclonal Antibody, 100ul Electrophoresis & Labeling Mutations in this gene resultThis gene encodes a protein that is a member of the syntaxin or t SNARE (target SNAP receptor) family. These proteins are found on cell membranes and serve as the targets for V SNARES (vesicle SNAP receptors) permitting specific synaptic vesicle docking and fusion. A microdeletion in the region of chromosome 20 where this gene is located has been associated with pseudohypoparathyroidism type Ib. Multiple transcript variants have been found for this