CD55 Polyclonal Antibody, 50ul[BT-AP01917] Plasma Mutations in this gene are

Mutations in this gene are associated with Hermansky-Pudlak syndrome type 5

May promote the rapid formation of a branched actin network by first nucleating new mother filaments and then activating Arp2/3 to branch off these filaments

and germinal center formation

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disease progression

CD55 Polyclonal Antibody, 50ul[BT-AP01917] Plasma Mutations in this gene areCOL1A2 encodes the pro alpha2 chain of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I IV, Ehlers Danlos syndrome type VIIB, recessive Ehlers Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan