Wiskott-Aldrich Syndrome 2 (WAS2)

Wiskott-Aldrich Syndrome 2, also known as wipf1 deficiency, is related to wiskott-aldrich syndrome and immune deficiency disease. An important gene associated with Wiskott-Aldrich Syndrome 2 is WIPF1 (WAS/WASL Interacting Protein Family Member 1). Affiliated tissues include nk cells and t cells, and related phenotypes are thrombocytopenia and eczema