dystrophia myotonica-protein kinase (DMPK)

Target Class
Official Symbol
Entrez Gene ID
Accession Number
Alias Names
DM; DM protein kinase; DM-kinase; DM1; DM1 protein kinase; DM1PK; DMK; MDPK; MT-PK; dystrophia myotonica-protein kinase; myotonic dystrophy associated protein kinase; myotonic dystrophy protein kinase; myotonin protein kinase A; myotonin-protein kinase; thymopoietin homolog
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 5-37 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 2008]
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Related Group Members: AGC

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KINOMEscan TKscan BROMOscan NHRscan GPCRscan PATHscan