DNER Polyclonal Antibody, 50ul Serological Pipets Mutations in this gene cause

Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome

CaMKV is thought to be catalytically inactive

and kidney

|Contains 5 Ig-like (immunoglobulin-like) domains

This gene is a member of the kelch-like family

DNER Polyclonal Antibody, 50ul Serological Pipets Mutations in this gene causeActivator of the NOTCH1 pathway. May mediate neuron glia interaction during astrocytogenesis.,Contains 1 follistatin like domain.,Contains 10 EGF like domains.,subcellular location: Present on the membrane of dendrites and cell bodies but excluded from axonal membrane. Also found in early endosomes in the somatodendritic region.,subunit: Interacts with AP1G1. Interacts with NOTCH1.,tissue specificity: Expressed in brain, spinal cord and adrenal gland.,