Pallidin is a protein that in humans is encoded by the PLDN gene.
The protein encoded by this gene may play a role in intracellular vesicle trafficking. It interacts with Syntaxin 13 which mediates intracellular membrane fusion. Mutations in this gene cause symptoms associated with Hermansky-Pudlak syndrome-9. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the X chromosome. [provided by RefSeq, Aug 2015].
via MyGene.info
Pallidin is a protein that in humans is encoded by the PLDN gene.
== Function ==
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).