The CHMP2B gene homepage

General information
Gene symbol CHMP2B
Gene name charged multivesicular body protein 2B
Chromosome 3
Chromosomal band p12.1
Imprinted Unknown
Genomic reference NG_007885.1
Transcript reference NM_014043.3
Associated with diseases ALS-17, FTD-3
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 44
Unique public DNA variants reported 28
Individuals with public variants 130
Hidden variants 0
Date created May 03, 2013
Date last updated February 08, 2021
Version CHMP2B:210208

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 24537
Entrez Gene 25978
PubMed articles CHMP2B
OMIM - Gene 609512
OMIM - Diseases ALS-17 (sclerosis, lateral, amyotrophic, type 17 (ALS-17))
FTD-3 (dementia, frontotemporal, chromosome 3-linked (FTD-3))
Orphanet CHMP2B

Active transcripts




NCBI ID     

NCBI Protein ID     

00005112 3 chromatin modifying protein 2B NM_014043.3 NP_054762.2 44

Copyright & disclaimer
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