Citations for
1DEPDC5, NPRL2, NPRL3
GATOR1 complex: the common genetic actor in focal epilepsies.
Baldassari S, Licchetta L, Tinuper P, Bisulli F, Pippucci T.
J Med Genet 53(8):503-10. doi: 10.1136/jmedgenet-2016-103883. Epub 2016 May 19. Review. 2016
2DEPDC5, FPEVF2
Preliminary functional assessment and classification of DEPDC5 variants associated with focal epilepsy.
van Kranenburg M, Hoogeveen-Westerveld M, Nellist M.
Hum Mutat 36(2):200-9. doi: 10.1002/humu.22723. Epub 2014 Nov 27. 2015
3DEPDC5, FPEVF2
DEPDC5 mutations in genetic focal epilepsies of childhood.
Lal D, Reinthaler EM, Schubert J, Muhle H, Riesch E, Kluger G, Jabbari K, Kawalia A, Bäumel C, Holthausen H, Hahn A, Feucht M, Neophytou B, Haberlandt E, Becker F, Altmüller J, Thiele H, Lemke JR, Lerche H, Nürnberg P, Sander T, Weber Y, Zimprich F, Neubauer BA.
Ann Neurol 75(5):788-92. doi: 10.1002/ana.24127. Epub 2014 Apr 14. 2014
4DEPDC5, FPEVF2
Novel DEPDC5 mutations causing familial focal epilepsy with variable foci identified.
Kaur A.
Clin Genet 84(4):341-2. doi: 10.1111/cge.12239. Epub 2013 Aug 21. No abstract available. 2013
5DEPDC5, FPEVF2
Mutations of DEPDC5 cause autosomal dominant focal epilepsies.
Ishida S, Picard F, Rudolf G, Noé E, Achaz G, Thomas P, Genton P, Mundwiller E, Wolff M, Marescaux C, Miles R, Baulac M, Hirsch E, Leguern E, Baulac S.
Nat Genet 45(5):552-5. doi: 10.1038/ng.2601. Epub 2013 Mar 31. 2013
6DEPDC5, FPEVF2
Mutations in DEPDC5 cause familial focal epilepsy with variable foci.
Dibbens LM, de Vries B, Donatello S, Heron SE, Hodgson BL, Chintawar S, Crompton DE, Hughes JN, Bellows ST, Klein KM, Callenbach PM, Corbett MA, Gardner AE, Kivity S, Iona X, Regan BM, Weller CM, Crimmins D, O'Brien TJ, Guerrero-López R, Mulley JC, Dubeau F, Licchetta L, Bisulli F, Cossette P, Thomas PQ, Gecz J, Serratosa J, Brouwer OF, Andermann F, Andermann E, van den Maagdenberg AM, Pandolfo M, Berkovic SF, Scheffer IE.
Nat Genet 45(5):546-51. doi: 10.1038/ng.2599. Epub 2013 Mar 31. 2013
7DEPDC5
Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers.
Miki D, Ochi H, Hayes CN, Abe H, Yoshima T, Aikata H, Ikeda K, Kumada H, Toyota J, Morizono T, Tsunoda T, Kubo M, Nakamura Y, Kamatani N, Chayama K.
Nat Genet 43(8):797-800. doi: 10.1038/ng.876. 2011
8C22orf24, DEPDC5, YWHAH
Complex chromosome 22 rearrangements in astrocytic tumors identified using microsatellite and chromosome 22 tile path array analysis.
Seng TJ, Ichimura K, Liu L, Tingby O, Pearson DM, Collins VP.
Genes Chromosomes Cancer 43(2):181-93. 2005
9AATK, ACIN1, ACOT11, ACSBG1, ADAMTS4, ADGRV1, AKAP11, ANKLE2, ARHGAP26, ARHGEF2, ASTN2, ATP2C2, ATP9A, BICD2, BZRAP1, C12orf51, CAND2, CEP135, CLASP1, CLASP2, CLUAP1, CLUH, CNOT3, COBL, CPNE3, CRTC1, CRY2, CSTF2T, CUL3, CUL4B, DAAM1, DAGLA, DEPDC5, DNAJC13, DOCK10, DZIP3, FBXW11, FKBP15, G3BP2, HEPH, HIP1R, HIPK1, ICOSLG, KIAA0649, KIAA0652, KIF13B, KIF1C, KIF21A, L3MBTL1, LDB3, MAGI2, MAP4K4, MFAP3L, MGEA5, MRC2, MTMR4, N4BP1, NPHP4, OBSL1, PAN2, PHACTR2, PHF2, PHLDB1, PLXND1, PPFIA3, PTCD1, RAB11FIP3, RBM19, RICH2, RNF40, RNF8, ROCK2, RRP12, SAPS2, SETX, SIN3B, SLC24A1, SMCHD1, SNAP91, SOCS5, SS18L1, SWAP70, TBC1D9B, TELO2, TNRC15, TSC22D2, UBE4B, UHRF1BP1L, ULK2, ZBED4, ZC3H11A, ZNF623
Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.
Ishikawa K, Nagase T, Suyama M, Miyajima N, Tanaka A, Kotani H, Nomura N,Ohara O.
DNA Res 5(3):169-76. 1998