NIPA2 Rabbit Polyclonal Antibody, 100ul Vector Construction It may also function as

It may also function as a redox-sensitive chaperone

Alterations of this gene| including point mutations| insertions and deletions| cause factor IX deficiency| which is a recessive X-linked disorder| also called hemophilia B or Christmas disease

The SET domain portion of this protein specifically methylates histone H3 lysines 4 and 36

Cdc7 is consistently expressed throughout the cell cycle

NIPA2 Rabbit Polyclonal Antibody, 100ul Vector Construction It may also function asThis gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3 7 and 21.