The MYLK2 gene homepage

General information
Gene symbol MYLK2
Gene name myosin light chain kinase 2
Chromosome 20
Chromosomal band q13.31
Imprinted Unknown
Genomic reference LRG_392
Transcript reference NM_033118.3
Exon/intron information NM_033118.3 exon/intron table
Associated with diseases CMH1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 97
Unique public DNA variants reported 69
Individuals with public variants 15
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated January 11, 2023
Version MYLK2:230111

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_033118.3.
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
HGNC 16243
Entrez Gene 85366
PubMed articles MYLK2
OMIM - Gene 606566
OMIM - Diseases CMH1 (cardiomyopathy, hypertrophic, familial, type 1)
GeneCards MYLK2
GeneTests MYLK2
Orphanet MYLK2

Active transcripts




NCBI ID     

NCBI Protein ID     

00014163 20 myosin light chain kinase 2 NM_033118.3 NP_149109.1 97

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