TM2D1
Description
The TM2D1 (TM2 domain containing 1) is a protein-coding gene located on chromosome 1.
This protein may play a role in cell death triggered by amyloid-beta, by interacting with the beta-APP42 protein. This interaction has been observed in studies documented in PubMed IDs 11278849 and 12836168.
TM2D1 is also known as BBP.
Associated Diseases
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- alpha thalassemia-intellectual disability syndrome type 1
- primary familial polycythemia due to EPO receptor mutation
