TBC1D15 Rabbit Polyclonal Antibody, 50ul Human Genome Knockout Libraries disease:A chromosomal aberration involving NUT

disease:A chromosomal aberration involving NUT is found in a rare

IRF1 serves as an activator of interferons alpha and beta transcription

An important paralog of this gene is NRIP3

Knockout studies in mice suggest that the different receptors

immunostimulatory

TBC1D15 Rabbit Polyclonal Antibody, 50ul Human Genome Knockout Libraries disease:A chromosomal aberration involving NUTThis gene encodes a member of the Ras like proteins in brain GTPase activating protein superfamily that share a conserved Tre 2 Bub2 Cdc16 domain. The encoded protein interacts with Ras like protein in brain 5A and may function as a regulator of intracellular trafficking. Alternate splicing results in multiple transcript variants.