USP17L19
Description
The USP17L19 (ubiquitin specific peptidase 17 like family member 19) is a protein-coding gene located on chromosome 4.
USP17L19 acts as a deubiquitinating enzyme, removing ubiquitin tags from specific proteins. This regulation impacts various cellular activities, potentially including cell growth, cell cycle progression, programmed cell death (apoptosis), cell movement, and the body's response to viral infections.
USP17L19 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
