USP17L20
Description
The USP17L20 (ubiquitin specific peptidase 17 like family member 20) is a protein-coding gene located on chromosome 4.
USP17L20 is a deubiquitinating enzyme that removes ubiquitin from proteins. This activity regulates various cellular processes, including cell proliferation, cell cycle progression, apoptosis, cell migration, and the cellular response to viral infection.
USP17L20 is also known as -.
Associated Diseases
- immunodeficiency 19
- combined immunodeficiency with skin granulomas
- immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
- severe combined immunodeficiency due to IKK2 deficiency
- ring chromosome Y
- severe combined immunodeficiency due to LAT deficiency
- obesity due to congenital leptin deficiency
- immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias
- immunodeficiency 105
- obesity due to leptin receptor gene deficiency
- spermatogenic failure 65
- common variable immunodeficiency
- immunodeficiency 18
- immunodeficiency 76
- spermatogenic failure 63
- Alzheimer disease
