MINAR2 and hearing loss, autosomal recessive 120: Recently, biallelic variants in the membrane integral NOTCH2-associated receptor 2 (MINAR2) gene were reported to cause autosomal recessive deafness-120 (DFNB120, OMIM#620238) in 13 patients (4 unrelated families) with nonsyndromic congenital (9 patients) or prelingual (4 patients), severe to profound SNHL, consistent with mouse and zebrafish model of MINAR2 ablation6.