The LMNB2 gene homepage

General information
Gene symbol LMNB2
Gene name lamin B2
Chromosome 19
Chromosomal band p13.3
Imprinted Unknown
Genomic reference NG_008355.1
Transcript reference NM_032737.3
Associated with diseases APLD
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 2
Unique public DNA variants reported 2
Individuals with public variants 1
Hidden variants 0
Date created May 03, 2013
Date last updated December 04, 2020
Version LMNB2:201204

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 6638
Entrez Gene 84823
PubMed articles LMNB2
OMIM - Gene 150341
OMIM - Diseases APLD (lipodystrophy, partial, acquired (APLD))
Orphanet LMNB2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00011447 19 lamin B2 NM_032737.3 NP_116126.3 2


Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective submitter(s) and curator(s) of the individual records. Individual data entries may indicate which data license applies to that specific record. When no license is listed, no permissions are granted. Any unauthorized use, copying, storage, or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2013-2021. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

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