ITB8 Polyclonal Antibody, 100ul Human Genome Knockout Libraries Mutations in this gene can

Mutations in this gene can cause X-linked eye disorders

AR contains 2 polymorphic trinucleotide repeat segments that encode polyglutamine and polyglycine tracts in the N-terminal transactivation domain of its protein

The encoded protein (trafficking protein particle complex 3) participates in the regulation of transport from the endoplasmic reticulum to the Golgi apparatus

member 4) family member in the same cluster

Mutations in this gene are associated with slow-channel congenital myasthenic syndrome

ITB8 Polyclonal Antibody, 100ul Human Genome Knockout Libraries Mutations in this gene canThis gene is a member of the integrin beta chain family and encodes a single pass type I membrane protein with a VWFA domain and four cysteine rich repeats. This protein noncovalently binds to an alpha subunit to form a heterodimeric integrin complex. In general, integrin complexes mediate cell cell and cell extracellular matrix interactions and this complex plays a role in human airway epithelial proliferation. Alternatively spliced variants which