FKBPL Polyclonal Antibody, 100ul Micro Centrifuge Tubes Mutations in this gene are

Mutations in this gene are associated with dolichol kinase deficiency

possibly a steroid

Mutations in this gene have been associated with nemaline myopathy (NM)| a rare congenital muscle disorder

A read-through transcript composed of SPECC1L (sperm antigen with calponin homology and coiled-coil domains 1-like) and the downstream ADORA2A (adenosine A2a receptor) gene sequence has been identified| but it is thought to be non-coding

The encoded protein tightly associates with cyclin-dependent kinase 9

FKBPL Polyclonal Antibody, 100ul Micro Centrifuge Tubes Mutations in this gene areThe protein encoded by FKBPL (FK506 binding protein like) has similarity to the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The encoded protein is thought to have a potential role in the induced radioresistance. Also it appears to have some involvement in the control of the cell cycle.