TReP-132 Polyclonal Antibody, 100ul Cellular Function Assays Mutations in HK1 have been

Mutations in HK1 have been associated with hemolytic anemia due to hexokinase deficiency

an autosomal recessive disorder characterized by unregulated insulin secretion

Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene

TRA2A is a member of the transformer 2 homolog family and encodes a protein with several RRM (RNA recognition motif) domains

including a secreted form

TReP-132 Polyclonal Antibody, 100ul Cellular Function Assays Mutations in HK1 have beenTRERF1 (transcriptional regulating factor 1) encodes a zinc finger transcriptional regulating protein which interacts with CBP p300 to regulate the human gene CYP11A1. Alternative splicing results in multiple transcript variants encoding different isoforms.