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CD55 Polyclonal Antibody, 50ul[BT-AP01917] Plasma Alternatively spliced transcript variants have

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CD55 Polyclonal Antibody, 50ul[BT-AP01917] Plasma Alternatively spliced transcript variants haveCOL1A2 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

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Description

Alternatively spliced transcript variants have been found for this gene that encode three distinct isoforms

and germinal center formation

GRK7 encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family

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

SDS3 is a subunit of the histone deacetylase (see HDAC1

CD55 Polyclonal Antibody, 50ul[BT-AP01917] Plasma Alternatively spliced transcript variants haveCOL1A2 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

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