Lamin B receptor

I wish to raise the following question:

Can lamin B receptor (LBR) be a candidate for “INM protein” in model 1 and/or 2?


Pathologically, LBR gene mutations are causative of Pelger-Huët anomaly, which is characterized by neutrophils with bilobed nuclei. (see, e.g., here and PLATE VIII-6 in Lichtman, M.A. et al. eds. Williams Hematology 7th ed. McGraw-Hill Medical 2005.)


Posted 08/28/07.