STX8 Rabbit Polyclonal Antibody, 20ul DNA Fragments Mutations in this gene result

Mutations in this gene result in one form of autosomal dominant hearing impairment

Polymorphisms in this gene may be associated with osteoarthritis in human patients

which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells

This protein is thought to protect centromeric cohesin from cleavage during mitotic prophase by preventing phosphorylation of a cohesin subunit

Gene Ontology (GO) annotations related to this gene include DNA-directed DNA polymerase activity

STX8 Rabbit Polyclonal Antibody, 20ul DNA Fragments Mutations in this gene resultThe gene is a member of the syntaxin family. The encoded protein is involved in protein trafficking from early to late endosomes via vesicle fusion and exocytosis. A related pseudogene has been identified on chromosome 12. Alternative splicing results in multiple transcript variants.