GPR25 Polyclonal Antibody, 100ul Apoptosis & Autophagy disease:Defects in MT-ND3 are a

disease:Defects in MT-ND3 are a cause of complex I mitochondrial respiratory chain deficiency

Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1)

facial dysmorphism

This protein interacts with PPARgamma

Multiple alternatively spliced transcript variants encoding different isoforms have been found for CAPN9

GPR25 Polyclonal Antibody, 100ul Apoptosis & Autophagy disease:Defects in MT-ND3 are aGPR25 is intronless and encodes a member of the G protein coupled receptor 1 family. G protein coupled receptors are membrane proteins which activate signaling cascades as a response to extracellular stress. GPR25 has been linked to arterial stiffness.