DYLT1 Polyclonal Antibody, 100ul Multiplex Immunoassays Mutations in this gene are

Mutations in this gene are a cause of congenital lipoid adrenal hyperplasia (CLAH)

It has also been called hepatic regenerative stimulation substance (HSS)

Plays an important role in the maintenance of the MICOS complex stability and the mitochondrial cristae morphology (PubMed: 22114354

permit disassembly of interphase structures and generation of M phase enzymatic activities and structures

1 that encodes an orphan G protein-coupled receptor

DYLT1 Polyclonal Antibody, 100ul Multiplex Immunoassays Mutations in this gene areThis gene encodes a component of the motor complex, cytoplasmic dynein, which transports cellular cargo along microtubules in the cell. The encoded protein regulates the length of primary cilia which are sensory organelles found on the surface of cells. The protein encoded by this gene interacts with viral proteins, like the minor capsid protein L2 of human papillomavirus, and is required for dynein mediated delivery of the viral nucleic acid to the