KLHL42 (Kelch Like Family Member 42) is a Protein Coding gene. Diseases associated with KLHL42 include Bardet-Biedl Syndrome 10. Among its related pathways are Innate Immune System and Class I MHC mediated antigen processing and presentation. Gene Ontology (GO) annotations related to this gene include ubiquitin-protein transferase activity. An important paralog of this gene is KLHL32.
Immunogen Information
Immunogen
Recombinant fusion protein of human KLHL42 (NP_065833.1).