NU6M Polyclonal Antibody, 100ul Apoptosis & Autophagy Disruption of this gene has

Disruption of this gene has been correlated with the autosomal dominant Marie Unna hereditary hypotrichosis disease

This protein has inhibin-like activity

This gene encodes a member of the CHD family of proteins which are characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains

6-biphosphatase enzymes

Two isoforms of CEP55 are expressed due to alternative splicing events

NU6M Polyclonal Antibody, 100ul Apoptosis & Autophagy Disruption of this gene hasCatalytic activity: NADH + ubiquinone = NAD(+) + ubiquinol.,disease: Defects in MT ND6 are a cause of Leber hereditary optic neuropathy (LHON)