NIPA2 Rabbit Polyclonal Antibody, 100ul Vector Construction Alterations of this gene| including

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

4 Mb region that is commonly deleted in diverse tumors

It was initially proposed that obestatin plays an opposing role to ghrelin by promoting satiety and thus decreasing food intake

sequence-specific DNA binding and RNA polymerase II transcription coactivator activity

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

NIPA2 Rabbit Polyclonal Antibody, 100ul Vector Construction Alterations of this gene| includingThis 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.