MNX1 Polyclonal Antibody, 20ul Microbial Genome Editing An important paralog of this

An important paralog of this gene is UBTD1

which leads to the loss in membrane potential and the release of cytochrome c

Hydrolyzes acetyl-CoA to acetate and CoA

highly hydrophobic N-terminal domain of 167 amino acids and a conserved C-terminal region of 299 amino acids

MNX1 Polyclonal Antibody, 20ul Microbial Genome Editing An important paralog of thisThis gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.