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) LOVD-team, but with Curator vacancy
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

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))


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00011447 19 lamin B2 NM_032737.3 NP_116126.3 1


Copyright & disclaimer
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