Automated description from the Alliance of Genome Resources (Release 7.4.0)
A structural constituent of cytoskeleton. Predicted to be involved in several processes, including heterochromatin formation; nucleus organization; and protein localization to nuclear envelope. Located in lamin filament and nuclear envelope. Is active in nuclear lamina. Is expressed in cortical plate; early conceptus; embryo; and retina outer nuclear layer. Human ortholog(s) of this gene implicated in partial lipodystrophy; primary autosomal recessive microcephaly; and progressive myoclonus epilepsy 9. Orthologous to human LMNB2 (lamin B2).
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