P2RX5-TAX1BP3
Description
The P2RX5-TAX1BP3 (P2RX5-TAX1BP3 readthrough (NMD candidate)) is a ncRNA gene located on chromosome 17.
The P2RX5-TAX1BP3 fusion gene is a rare genetic variant that has been identified in some individuals with cancer. It is formed by the joining of the P2RX5 and TAX1BP3 genes, resulting in a chimeric protein with the potential to disrupt normal cellular function.
The P2RX5-TAX1BP3 fusion gene is a rare genetic variant that is associated with a specific type of cancer. It is thought to contribute to the development of the disease by disrupting normal cellular processes.
P2RX5-TAX1BP3 is also known as P2RX5, P2X5.
Associated Diseases
- severe combined immunodeficiency due to IKK2 deficiency
- brain cancer
- type 2 diabetes mellitus
- urinary bladder carcinoma
- cancer
- cervical squamous intraepithelial neoplasia
- cystic fibrosis
- Aarskog-Scott syndrome, X-linked
