NETO1 Polyclonal Antibody, 20ul Thermal Control Defects in this gene are

Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD)

Belongs to the grh/CP2 family

Interactions between this protein and the sarcomeric proteins myopalladin and titin suggest that it may also be involved in the myofibrillar stretch-sensor system

This gene is involved in a specific translocation event that creates a fusion of this gene and the RNA-binding motif protein-15 gene

NETO1 Polyclonal Antibody, 20ul Thermal Control Defects in this gene areThis gene encodes a predicted transmembrane protein containing two extracellular CUB domains followed by a low density lipoprotein class A (LDLa) domain. A similar gene in mice encodes a protein that plays a critical role in spatial learning and memory by regulating the function of synaptic N methyl D aspartic acid receptor complexes in the hippocampus. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this