Lamin B2

LMNB2
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2LLL, 5BNW
Identifiers
Aliases	LMNB2, lamin B2, LAMB2, LMN2, EPM9, MCPH27
External IDs	OMIM: 150341; MGI: 96796; HomoloGene: 7818; GeneCards: LMNB2; OMA:LMNB2 - orthologs
Gene location (Human)
Chr.	Chromosome 19 (human)
End	2,456,959 bp
Gene location (Mouse)
Chr.	Chromosome 10 (mouse)
End	80,754,079 bp
RNA expression pattern
	Top expressed in
	ventricular zone; ; left testis; ; right testis; ; ganglionic eminence; ; secondary oocyte; ; stromal cell of endometrium; ; mucosa of transverse colon; ; mucosa of esophagus; ; muscle of thigh; ; gastrocnemius muscle;
	Top expressed in
	spermatid; ; seminiferous tubule; ; ventricular zone; ; epiblast; ; cumulus cell; ; embryo; ; yolk sac; ; granulocyte; ; neural layer of retina; ; renal corpuscle;
	More reference expression data
	n/a
Gene ontology
Molecular function	structural molecule activity; protein binding; molecular function;
Cellular component	intermediate filament; nucleus; membrane; nuclear inner membrane; lamin filament; nuclear envelope; nuclear membrane;
Biological process	biological process;
	Sources:Amigo / QuickGO
Orthologs
	84823
	16907
	ENSG00000176619
	ENSMUSG00000062075
	Q03252
	P21619
	NM_032737
	NM_010722; NM_001347140
	NP_116126
	NP_001334069; NP_034852
	Wikidata
View/Edit Human	View/Edit Mouse

Lamin B2 is a protein that in humans is encoded by the LMNB2 gene. It is the second of two type B nuclear lamins, and it is associated with laminopathies.