C1QT5 Polyclonal Antibody, 20ul Immune Cell Analysis Mutations in this gene are

Mutations in this gene are the cause of several cardiomyopathies and keratodermas| including skin fragility-woolly hair syndrome

ACVR1B encodes an activin A type IB receptor

has been defined for this gene

FOXB1 is a gene on chromosome 15q22 that encodes a member of the forkhead class of DNA-binding proteins

It participates in apoptosis signaling through highly specific protein-protein homophilic interactions

C1QT5 Polyclonal Antibody, 20ul Immune Cell Analysis Mutations in this gene areThis gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequence from the upstream membrane frizzled related protein gene (MFRP), or by a monocistronic transcript expressed from an internal promoter.