SYT8 Polyclonal Antibody, 100ul Metabolic enzymes tool compounds Mutations in RAB3GAP1 are associated

Mutations in RAB3GAP1 are associated with Warburg micro syndrome

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also referred to as autosomal dominant atrophic macular degeneration

and a carboxyl-terminal guanylyl cyclase catalytic domain

ChemR23 is highly expressed in developing osseous and cartilaginous tissue

SYT8 Polyclonal Antibody, 100ul Metabolic enzymes tool compounds Mutations in RAB3GAP1 are associatedThis gene encodes a member of the synaptotagmin protein family. Synaptotagmins are membrane proteins that are important in neurotransmission and hormone secretion, both of which involve regulated exocytosis. Expression of the encoded protein in human pancreatic islets has been connected to activity of the promoter for the insulin gene, on the same chromosome several hundred kilobases away (PMID: 21336277 and 22928559). This association would link