Gene symbol and protein | Gene Location | All allelic disease phenotypes - locus/disease symbols |
HNRNPA2B1 Hetergeneous nuclear ribonucleoprotein A2/B1       | 7q15.2 | * Oculopharyngeal muscular dystrophy related to HNRNPA2B1 - (5.26, 5.36)* Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia - IBMPFD2 (5.26, 5.36) |