View gene DNM2

This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp).
General information
Gene symbol DNM2
Gene name dynamin 2
Chromosome 19
Chromosomal band p
Imprinted Unknown
Genomic reference NG_008792.1
Transcript reference NM_001005360.2
Associated with diseases CMTDIB, CNM-1, LCCS-5
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (2) Fleur Garton and Johan den Dunnen
Total number of public variants reported 49
Unique public DNA variants reported 33
Individuals with public variants 144
Hidden variants 0
Notes This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp).
Date created May 01, 2010
Date last updated December 12, 2015
Version DNM2:151212

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
Homepage URL http://www.LOVD.nl/DNM2
HGNC 2974
Entrez Gene 1785
PubMed articles DNM2
OMIM - Gene 602378
OMIM - Diseases CMTDIB (CMT-2M)
CNM-1 (myopathy, centronuclear, type 1 (CNM-1))
LCCS-5 (contracture syndrome, lethal, congenital, type 5 (LCCS-5))
HGMD DNM2
GeneCards DNM2
GeneTests DNM2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00023873 19 transcript variant 1 NM_001005360.2 NP_001005360.1 49


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