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Search results 1 to 1 out of 1 for Trps1

Category restricted to ProteinDomain (x)

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Category: ProteinDomain
Type Details Score
Protein Domain
Type: Family
Description: The TRPS1 gene encodes a multi zinc-finger nuclear regulator of chondrocyte proliferation and differentiation []. Mutations in the gene cause trichorhinophalangeal syndrome (TRPS), an autosomal dominant skeletal dysplasia []. The Trps1 protein also acts as regulator of histone deacetylation, interacting with two histone deacetylases, Hdac1 and Hdac4, thereby increasing their activity [].