FoxD4L1 Polyclonal Antibody, 20ul Cell fragmentation and collection Mutations in this gene result

Mutations in this gene result in Birbeck granules deficiency or loss of sugar binding activity

proteolytic cleavage of the non-collagenous carboxy-terminal domain results in a biologically active fragment known as arresten

Heterodimers consisting of alpha and gamma subunits have also been described

Mutations in CTSD play a causal role in neuronal ceroid lipofuscinosis-10 and may be involved in the pathogenesis of several other diseases

and is thought to be a member of the secretin receptor family

FoxD4L1 Polyclonal Antibody, 20ul Cell fragmentation and collection Mutations in this gene resultFOXD4L1 is a member of the forkhead winged helix (FOX) family of transcription factors with highly conserved FOX DNA binding domains. Members of the FOX family of transcription factors are regulators of embryogenesis and may play a role in human cancer. This gene lies in a region of chromosome 2 that surrounds the site where two ancestral chromosomes fused to form human chromosome 2. This region is duplicated elsewhere in the human genome, primarily