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LMNB2 gene

lamin B2

Key facts

Official symbol
LMNB2
Full name
LMNB2
Chromosome
19
Map location
19p13.3
Organism
Homo sapiens
NCBI Gene ID
84823
Also known as
EPM9, LAMB2, LMN2, MCPH27

Function summary

This gene encodes a B type nuclear lamin. The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Mutations in this gene are associated with acquired partial lipodystrophy. [provided by RefSeq, May 2012].

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Data source: NCBI Gene · alsesAI Gene Library