AMPO Polyclonal Antibody, 20ul Cell Transfection Mutation in this gene causes

Mutation in this gene causes dimethylglycine dehydrogenase deficiency

The human galanin receptors are G protein-coupled receptors that functionally couple to their intracellular effector through distinct signaling pathways

disease:A chromosomal rearrangement involving CTNNB1 may be a cause of salivary gland pleiomorphic adenomas (PA)

A similar protein in budding yeast is a component of pre-60S ribosomal particles| and is required for the early maturation steps of the 60S subunit

Ectonucleotide pyrophosphatase/phosphodiesterase family member 3 encoded by ENPP3 belongs to a series of ectoenzymes that are involved in hydrolysis of extracellular nucleotides

AMPO Polyclonal Antibody, 20ul Cell Transfection Mutation in this gene causesThis gene encodes a member of the M1 zinc aminopeptidase family. The encoded protein is a zinc dependent metallopeptidase that catalyzes the removal of an amino acid from the amino terminus of a protein or peptide. This protein may play a role in the generation of angiotensin IV. Alternate splicing results in multiple transcript variants.