Predicted to be a structural constituent of cytoskeleton. Predicted to be involved in cellular localization; heterochromatin formation; and nucleus organization. Located in apical cortex; cell junction; and terminal web. Expressed in intestine. Human ortholog(s) of this gene implicated in partial lipodystrophy; primary autosomal recessive microcephaly; and progressive myoclonus epilepsy 9. Is an ortholog of human LMNB2 (lamin B2).
Is predicted to encode a protein with the following domains: Lamin tail domain superfamily; Intermediate filament protein; Intermediate filament, ifa/ifb; and Intermediate filament, rod domain. Is an ortholog of C. elegans ifb-2.
Is predicted to encode a protein with the following domains: Lamin tail domain superfamily; Intermediate filament protein; Intermediate filament, ifa/ifb; and Intermediate filament, rod domain. Is an ortholog of C. elegans ifb-2.
Is predicted to encode a protein with the following domains: Lamin tail domain superfamily; Intermediate filament protein; Intermediate filament, ifa/ifb; and Intermediate filament, rod domain. Is an ortholog of C. elegans ifb-2.
Is predicted to encode a protein with the following domains: Lamin tail domain superfamily; Intermediate filament protein; Intermediate filament, ifa/ifb; and Intermediate filament, rod domain. Is an ortholog of C. elegans ifb-2.
Predicted to be a structural constituent of cytoskeleton. Predicted to be involved in cellular localization; heterochromatin formation; and nucleus organization. Located in apical plasma membrane. Expressed in several structures, including egg-laying apparatus; excretory system; pharyngeal-intestinal valve; pharynx; and somatic nervous system. Human ortholog(s) of this gene implicated in partial lipodystrophy; primary autosomal recessive microcephaly; and progressive myoclonus epilepsy 9. Is an ortholog of human LMNB2 (lamin B2).
Is predicted to encode a protein with the following domains: Lamin tail domain superfamily; Intermediate filament protein; Intermediate filament, ifa/ifb; and Intermediate filament, rod domain. Is an ortholog of C. elegans ifb-2.
Predicted to be a structural constituent of cytoskeleton. Involved in cell-cell adhesion. Located in hemidesmosome. Expressed in hypodermis; touch receptor neurons; uterus; and ventral cord neurons. Human ortholog(s) of this gene implicated in partial lipodystrophy; primary autosomal recessive microcephaly; and progressive myoclonus epilepsy 9. Is an ortholog of human LMNB2 (lamin B2).