TOM1-like protein 2 is a protein that in humans is encoded by the TOM1L2 gene.
This gene belongs to a small gene family whose members have an N-terminal VHS domain followed by a GAT domain; domains which typically participate in vesicular trafficking. The canonical protein encoded by this gene also has a C-terminal clathrin binding motif. This protein has been shown to interact with Tollip, clathrin and ubiquitin and is thought to play a role in endosomal sorting. This gene resides in the 3.7 Mb deletion of chromosome region 17p11.2 that is associated with Smith-Magenis syndrome. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Apr 2017].
via MyGene.info
TOM1-like protein 2 is a protein that in humans is encoded by the TOM1L2 gene.
==See also== TOM1, target of Myb1 membrane trafficking protein TOM1L1
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).