ITGA2B Rabbit Polyclonal Antibody, 100ul[BT-AP10696] Diagnostic Probes & Oligos |disease:Defects in F7 are the

|disease:Defects in F7 are the cause of factor VII deficiency

and unlike most other members of this family

SH3TC1 (SH3 Domain And Tetratricopeptide Repeats 1) is a Protein Coding gene

The protein encoded by this gene plays important roles in the determination of centrosome position and segregation

Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta

ITGA2B Rabbit Polyclonal Antibody, 100ul[BT-AP10696] Diagnostic Probes & Oligos |disease:Defects in F7 are theThis gene encodes a member of the integrin alpha chain family of proteins. The encoded preproprotein is proteolytically processed to generate light and heavy chains that associate through disulfide linkages to form a subunit of the alpha IIb beta 3 integrin cell adhesion receptor. This receptor plays a crucial role in the blood coagulation system by mediating platelet aggregation. Mutations in this gene are associated with platelet type bleeding