Citations for
1DDX54, DHX16, DHX34, DHX37, DHX38, NDDNA, NDDNA2, NDDNA3, NDDRA, RP84
Paralog Studies Augment Gene Discovery: DDX and DHX Genes.
Paine I, Posey JE, Grochowski CM, Jhangiani SN, Rosenheck S, Kleyner R, Marmorale T, Yoon M, Wang K, Robison R, Cappuccio G, Pinelli M, Magli A, Coban Akdemir Z, Hui J, Yeung WL, Wong BKY, Ortega L, Bekheirnia MR, Bierhals T, Hempel M, Johannsen J, Santer R, Aktas D, Alikasifoglu M, Bozdogan S, Aydin H, Karaca E, Bayram Y, Ityel H, Dorschner M, White JJ, Wilichowski E, Wortmann SB, Casella EB, Kitajima JP, Kok F, Monteiro F, Muzny DM, Bamshad M, Gibbs RA, Sutton VR; University of Washington Center for Mendelian Genomics, Baylor-Hopkins Center for Mendelian Genomics, Telethon Undiagnosed Diseases Program, Van Esch H, Brunetti-Pierri N, Hildebrandt F, Brautbar A, Van den Veyver IB, Glass I, Lessel D, Lyon GJ, Lupski JR.
Am J Hum Genet 105(2):302-316. doi: 10.1016/j.ajhg.2019.06.001. Epub 2019 Jun 27. 2019
2DHX38
DEAH box RNA helicase DHX38 associates with satellite I noncoding RNA involved in chromosome segregation.
Nishimura K, Cho Y, Tokunaga K, Nakao M, Tani T, Ideue T.
Genes Cells 24(8):585-590. doi: 10.1111/gtc.12707. Epub 2019 Jun 28. 2019
3DHX38, RP84
Confirmation of the Role of DHX38 in the Etiology of Early-Onset Retinitis Pigmentosa.
Latif Z, Chakchouk I, Schrauwen I, Lee K, Santos-Cortez RLP, Abbe I, Acharya A, Jarral A, Ali I, Ullah E, Khan MN, Ali G, Tahir TH, Bamshad MJ, Nickerson DA, Ahmad W, Ansar M, Leal SM; University of Washington Center for Mendelian Genomics (UWCMG) Study Group.
Invest Ophthalmol Vis Sci 59(11):4552-4557. doi: 10.1167/iovs.18-23849. 2018
4DHX38
Mutations in spliceosomal proteins and retina degeneration.
Růžičková Š, Staněk D.
RNA Biol 14(5):544-552. doi: 10.1080/15476286.2016.1191735. Epub 2016 Jun 14. Review. 2017
5DHX38, RP84
A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma.
Ajmal M, Khan MI, Neveling K, Khan YM, Azam M, Waheed NK, Hamel CP, Ben-Yosef T, De Baere E, Koenekoop RK, Collin RW, Qamar R, Cremers FP.
J Med Genet 51(7):444-8. doi: 10.1136/jmedgenet-2014-102316. Epub 2014 Apr 15. 2014
6DHX16, DHX38, GPKOW, PRPF8, PRPF8, SLU7
Dynamic protein-protein interaction wiring of the human spliceosome.
Hegele A, Kamburov A, Grossmann A, Sourlis C, Wowro S, Weimann M, Will CL, Pena V, Lührmann R, Stelzl U.
Mol Cell 45(4):567-80. doi: 10.1016/j.molcel.2011.12.034. 2012
7DHX38, SLU7
DEAH-box ATPase Prp16 has dual roles in remodeling of the spliceosome in catalytic steps.
Tseng CK, Liu HL, Cheng SC.
RNA 17(1):145-54. doi: 10.1261/rna.2459611. Epub 2010 Nov 22. 2011
8DHX38, ISY1
The Isy1p component of the NineTeen complex interacts with the ATPase Prp16p to regulate the fidelity of pre-mRNA splicing.
Villa T, Guthrie C.
Genes Dev 19(16):1894-904. 2005
9DDX23, DDX27, DDX31, DDX41, DDX42, DDX43, DDX46, DDX47, DDX49, DDX50, DDX51, DDX52, DDX53, DDX54, DDX55, DDX56, DHX15, DHX29, DHX30, DHX32, DHX33, DHX34, DHX35, DHX36, DHX37, DHX38, DHX40, DHX57, DHX8, DHX9, EIF4A2, EIF4A3
The human DDX and DHX gene families of putative RNA helicases.
Abdelhaleem M, Maltais L, Wain H.
Genomics 81(6):618-22. 2003
10ABCC11, ABCC6P1, ABCC6P2, ACYP2, APOB48R, CCL22, CCP110, CDC37, CIAPIN1, CLN3, COQ9, CX3CL1, CXCR3, DDX28, DHX38, DOK4, EARS2, EARS2, EIF3CL, GDE1, GTF3C1, LKAP, MAZ, NOMO1, NOMO2, NPIPA1, NUPR1, ORIPL, PMFBP1, RBKH, SLC7A5P1, TCCK, UBFD1, XPO6, ZG16, ZP2
Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q.
Loftus BJ, Kim UJ, Sneddon VP, Kalush F, Brandon R, Fuhrmann J, Mason T,Crosby ML, Barnstead M, Cronin L, Deslattes Mays A, Cao Y, Xu RX, Kang HL,Mitchell S, Eichler EE, Harris PC, Venter JC, Adams MD.
Genomics 60(3):295-308. 1999
11DHX38
PRP16, a DEAH-box RNA helicase, is recruited to the spliceosome primarily via its nonconserved N-terminal domain.
Wang Y, Guthrie C.
RNA 4(10):1216-29. 1998
12CDC40, DHX38
Human homologs of yeast prp16 and prp17 reveal conservation of the mechanism for catalytic step II of pre-mRNA splicing.
Zhou Z, Reed R.
EMBO J 17(7):2095-106. 1998
13ANKS1A, BCL2L2, DCUN1D4, DHX38, DHX38, DVL3, EDEM1, FAM38A, FIG4, GCN1L1, HSPH1, IHPK1, KIAA0232, KIAA0240, KIAA0247, LARP4B, LPGAT1, LRRC8B, MFN2, MRPS27, NCSTN, NUP205, PHF15, PHF16, PHYHIP, PIEZO1, PUM2, RAPGEF5, RGP1, RIMS3, RNF10, RTF1, RUBCN, SNX19, SPOCK2, STAB1, TATDN2, TBC1D5, TIAF1, TM9SF4, TOPBP1, WAPL, WASF1, ZNF516, ZNF516, ZNF592
Prediction of the coding sequences of unidentified human genes. VI. the coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain.
Nagase T, et al.
DNA Res 3 : 321-329,341-54. 1996