Lmnb2 - lamin B2

Predicted to enable identical protein binding activity. Predicted to be located in lamin filament and nuclear membrane. 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). [provided by Alliance of Genome Resources, Apr 2022]