GPR89B
Description
The GPR89B (G protein-coupled receptor 89B) is a protein-coding gene located on chromosome 1.
The GPR89B gene in humans encodes the protein GPR89.
GPR89B is also known as GPHR, GPR89, GPR89C, LINC02804, SH120, UNQ192.
Associated Diseases
- Okt4 epitope deficiency
- combined immunodeficiency with skin granulomas
- peptic ulcer disease
- 22q11.2 deletion syndrome
- immunodeficiency 19
- immunodeficiency 18
- breast cancer
