• Thumbnail for DDX3X
    ATP-dependent RNA helicase DDX3X is an enzyme that in humans is encoded by the DDX3X gene. DEAD box proteins are putative RNA helicases characterized...
    17 KB (1,788 words) - 09:39, 10 October 2024
  • DDX3X syndrome is a genetic disorder that affects predominantly females. Patients with DDX3X syndrome may develop developmental delay or intellectual disability...
    3 KB (415 words) - 15:15, 14 June 2024
  • Thumbnail for Burkitt lymphoma
    sequential mutations of the RNA helicases (involved in RNA synthesis) DDX3X (found on the x chromosome) and DDX3Y (found on the y chromosome) lead to...
    38 KB (4,416 words) - 08:01, 25 August 2024
  • Thumbnail for Extranodal NK/T-cell lymphoma, nasal type
    (e.g. tofacitinib), JAK1/JAK2 (e.g. AZD1480), STAT3 (e.g. WP1066), and DDX3X (e.g. RK-33) are being study in pre-clinical in vitro experiments as potential...
    46 KB (5,496 words) - 23:40, 12 October 2024
  • Thumbnail for Y chromosome
    counterparts escape inactivation. USP9Y USP9X Ubiquitin protease. DDX3Y DDX3X Helicase. UTY UTX Histone demethylase. TB4Y TB4X AZFb (none) Second AZF...
    81 KB (8,153 words) - 17:25, 22 September 2024
  • Thumbnail for Helicase
    CHD3, CHD4, CHD5, CHD6, CHD7, CHD8, CHD9 DEAD box/DEAD/DEAH box helicase: DDX3X, DDX5, DDX6, DDX10, DDX11, DDX12, DDX58, DHX8, DHX9, DHX37, DHX40, DHX58...
    56 KB (6,916 words) - 17:01, 27 August 2024
  • HGNC:2732 P30046 4074 DDTL HGNC:33446 A6NHG4 4075 DDX1 HGNC:2734 Q92499 4076 DDX3X HGNC:2745 O00571 4077 DDX3Y HGNC:2699 O15523 4078 DDX4 HGNC:18700 Q9NQI0...
    277 KB (17 words) - 18:34, 6 October 2024
  • Thumbnail for DDX3Y
    gene encodes a DEAD box protein, and it has a homolog on the X chromosome (DDX3X). The gene mutation causes male infertility, Sertoli cell-only syndrome...
    7 KB (876 words) - 03:52, 1 April 2024
  • de novo mutations in a set of genes. Mutations in three of these genes (DDX3X, TLK2 and HDAC8) were shared with those found in databases of individuals...
    6 KB (598 words) - 11:20, 24 August 2024
  • Thumbnail for Medulloblastoma
    syndrome. Recurrent mutations in the genes CTNNB1, PTCH1, MLL2, SMARCA4, DDX3X, CTDNEP1, KDM6A, and TBR1 were identified in individuals with medulloblastoma...
    36 KB (3,455 words) - 22:51, 26 April 2024