Also known as PMRED, Smad nuclear interacting protein 1, PML1, NEDHCS
Smad nuclear-interacting protein 1 is a protein that in humans is encoded by the SNIP1 gene.
This gene encodes a protein that contains a coiled-coil motif and C-terminal forkhead-associated (FHA) domain. The encoded protein functions as a transcriptional coactivator that increases c-Myc activity and inhibits transforming growth factor beta (TGF-beta) and nuclear factor kappa-B (NF-kB) signaling. The encoded protein also regulates the stability of cyclin D1 mRNA, and may play a role in cell proliferation and cancer progression. Mutations in this gene are a cause of psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED). [provided by RefSeq, Mar 2012].
via MyGene.info
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Smad nuclear-interacting protein 1 is a protein that in humans is encoded by the SNIP1 gene.
== Interactions ==
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).