DMPK Chromosome 19

DM1 protein kinase
1 variant 1 Health Risk

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What This Gene Does
The protein encoded by this gene is a serine-threonine kinase that is closely related to other kinases that interact with members of the Rho family of small GTPases. Substrates for this enzyme include myogenin, the beta-subunit of the L-type calcium channels, and phospholemman. The 3' untranslated region of this gene contains 5-38 copies of a CTG trinucleotide repeat. Expansion of this unstable motif to 50-5,000 copies causes myotonic dystrophy type I, which increases in severity with increasing repeat element copy number. Repeat expansion is associated with condensation of local chromatin structure that disrupts the expression of genes in this region. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2016]
Gene Info
Gene Group
DMPK kinase family
Locus Type
gene with protein product
Location
19q13.32
Ensembl
ENSG00000104936
Associated Conditions (1)
Inborn genetic diseases
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS758732755 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
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