HXK I Polyclonal Antibody, 100ul Molecular Sciences or in an active form

or in an active form consisting solely of the mature peptide homodimer

Mutations in MYOZ2 cause cardiomyopathy familial hypertrophic type 16

This gene encodes a single-pass membrane protein| which contains a conserved sequence of the GCN5 or NAT superfamily of N-acetyltransferases and is a member of the N-acyltransferase (NAT) superfamily

3'-end processing

HXK I Polyclonal Antibody, 100ul Molecular Sciences or in an active formHexokinases phosphorylate glucose to produce glucose 6 phosphate, the first step in most glucose metabolism pathways. HK1 encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria. Mutations in HK1 have been associated with hemolytic anemia due to hexokinase deficiency. Alternative splicing of this gene results in several transcript variants which encode different isoforms, some of which are tissue specific.