HNRNPA2B1 is a protein with 37 kDa. Has various molecular functions, such as identical protein binding. Is involved in several biological processes, including RNA metabolic process.
Inclusion body myopathy with early-onset Paget disease
Used cell type
HeLa, HEK293, fibroblasts
Used Stimuli
Sodium arsenite
Subcellular Localization
Nucleus, exosome, Cytoplasmic granule
Reference
Kim, H. J., Kim, N. C., Wang, Y.-D., Scarborough, E. A., Moore, J., Diaz, Z., … Taylor, J. P. (2013). Prion-like domain mutations in hnRNPs cause multisystem proteinopathy and ALS. Nature, 495(7442), 467–473