DYM Rabbit Polyclonal Antibody, 100ul Cell fragmentation and collection Defects in this gene have

Defects in this gene have been associated with idiopathic dilated cardiomyopathy (IDC) and familial hypertrophic cardiomyopathy (FHC)

and involvement in cargo sorting during receptor endocytosis

Most MS4A genes| including MS4A10| encode proteins with at least 4 potential transmembrane domains and N- and C-terminal cytoplasmic domains encoded by distinct exons

induction:Detected at low levels at interphase and in resting cells

DYM Rabbit Polyclonal Antibody, 100ul Cell fragmentation and collection Defects in this gene haveThis gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia Dyggve Melchior Clausen (DMC) dysplasia and Smith McCort (SMC) dysplasia which involve both skeletal defects and mental retardation.