FAM136A Knockout Cell Line-293T

CSC-RT0174

293T-FAM136A (-/-) is a stable cell line with a homozygous knockout of human FAM136A

293T

Human

This gene encodes a mitochondrially localized protein that is highly conserved across species. The gene is expressed in a variety of tissues including human lymphoblast cells and rat neurosensorial epithelium of the cristaampullaris. A mutation in this gene has been associated with familial Menieres disease, a chronic disorder of the inner ear. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]