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)[1] Band 19p13.3 Start 2,427,638 bp[1] End 2,456,959 bp[1]
Gene location (Mouse) Chr. Chromosome 10 (mouse)[2] Band 10 C1|10 39.72 cM Start 80,737,037 bp[2] End 80,754,079 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in Top expressed in More reference expression data BioGPS n/a
Gene ontology Molecular function Cellular component Biological process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 84823 16907 Ensembl ENSG00000176619 ENSMUSG00000062075 UniProt Q03252 P21619 RefSeq (mRNA) NM_032737 NM_010722 NM_001347140 RefSeq (protein) NP_116126 NP_001334069 NP_034852 Location (UCSC) Chr 19: 2.43 – 2.46 Mb Chr 10: 80.74 – 80.75 Mb PubMed search [3] [4]
Wikidata
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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.

• Lamin B receptor
• Barraquer–Simons syndrome
• Pelger–Huët anomaly

• Lamin+B at the U.S. National Library of Medicine Medical Subject Headings (MeSH)