USP17L22
Description
The USP17L22 (ubiquitin specific peptidase 17 like family member 22) is a protein-coding gene located on chromosome 4.
USP17L22 is a deubiquitinating enzyme that removes ubiquitin tags from specific proteins. This process regulates various cellular processes, potentially affecting cell proliferation, cell cycle progression, apoptosis, cell migration, and the cell's response to viral infections.
USP17L22 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
