Applications: WB, ELISA, PA, AP
The MN1 gene, which resides on chromosome 22, encodes a 1,319 amino acid protein. The ETV6/TEL gene has been reported to fuse to MN1. The MN1-TEL fusion protein, encoded by the translocation (12;22)(p13;q11) in myeloid leukemia, is a transcription factor with transforming activity. Defects in MN1 (meningioma 1) may be a cause of meningiomas, slowly growing benign tumors derived from the arachnoidal cap cells of the leptomeninges, the soft coverings of the brain and spinal cord.
|Product By Gene ID
- probable tumor suppressor protein MN1
- meningioma chromosome region
- meningioma chromosome region 1
- meningioma (translocation balanced)
- meningioma (disrupted in balanced translocation) 1
Research Areas for MN1
Find related products by research area and learn more about each of the different research areas below.Cell Cycle and Replication
Bioinformatics Tool for MN1
Discover related pathways, diseases and genes to MN1. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.