DPP10 Polyclonal Antibody, 50ul Cell Dissociation Defects in this gene can

Defects in this gene can also cause cone-rod dystrophy type 11| a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity| followed by the degeneration of rod photoreceptor cells| which progresses to night blindness and the loss of peripheral vision

This gene functions in the regulation of autophagy

Read-through transcription also exists between this gene and the downstream WFDC6 (WAP four-disulfide core domain 6) gene

The phospholipase D family member 3 is a single-pass type II membrane protein and contains two PLD phosphodiesterase domains

Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints

DPP10 Polyclonal Antibody, 50ul Cell Dissociation Defects in this gene canThis gene encodes a single pass type II membrane protein that is a member of the S9B family in clan SC of the serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally present in the catalytic domain of serine proteases. However, it does bind specific voltage gated potassium channels and alters their expression and biophysical properties. Mutations in this gene have been