DMPK Polyclonal Antibody, 50ul Mini dry bath human MEGF9 shares 76% aa

human MEGF9 shares 76% aa sequence identity with mouse MEGF9

Mutations in this gene cause cranioectodermal dysplasia-1

alternatively spliced transcript variants encoding a range of isoforms have been described

May interact with NOM1

The protein encoded by this gene contains two FH domains and belongs to a novel FH protein subfamily implicated in cell polarity

DMPK Polyclonal Antibody, 50ul Mini dry bath human MEGF9 shares 76% aaDystrophia myotonica protein kinase encoded by DMPK 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