Citations for
1CHCHD2, DNAJC13, DNAJC6, PARK19, PARK21, PARK22, PARKX, RAB39B, TMEM230
New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.
Puschmann A.
Curr Neurol Neurosci Rep 17(9):66. doi: 10.1007/s11910-017-0780-8. Review. 2017
2CLN4B, DNAJC13, DNAJC5, DNAJC6
The Role of Co-chaperones in Synaptic Proteostasis and Neurodegenerative Disease.
Gorenberg EL, Chandra SS.
Front Neurosci 11:248. doi: 10.3389/fnins.2017.00248. eCollection 2017. Review. 2017
3DNAJC13, PARK21
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease.
Ross JP, Dupre N, Dauvilliers Y, Strong S, Ambalavanan A, Spiegelman D, Dionne-Laporte A, Pourcher E, Langlois M, Boivin M, Leblond CS, Dion PA, Rouleau GA, Gan-Or Z.
Neurobiol Aging 45:212.e13-212.e17. doi: 10.1016/j.neurobiolaging.2016.04.023. Epub 2016 May 3. 2016
4DNAJC13, PARK21
DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.
Lorenzo-Betancor O, Ogaki K, Soto-Ortolaza AI, Labbe C, Walton RL, Strongosky AJ, van Gerpen JA, Uitti RJ, McLean PJ, Springer W, Siuda J, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, McCarthy A, Lynch T, Puschmann A, Rektorova I, Sanotsky Y, Vilariño-Güell C, Farrer MJ, Ferman TJ, Boeve BF, Petersen RC, Parisi JE, Graff-Radford NR, Dickson DW, Wszolek ZK, Ross OA.
Eur J Neurol 22(9):1323-5. doi: 10.1111/ene.12770. 2015
5DNAJC13, PARK21
VPS35 and DNAJC13 disease-causing variants in essential tremor.
Rajput A, Ross JP, Bernales CQ, Rayaprolu S, Soto-Ortolaza AI, Ross OA, van Gerpen J, Uitti RJ, Wszolek ZK, Rajput AH, Vilariño-Güell C.
Eur J Hum Genet 23(6):887-8. doi: 10.1038/ejhg.2014.164. Epub 2014 Aug 13. 2015
6DNAJC13
Receptor-mediated Endocytosis 8 Utilizes an N-terminal Phosphoinositide-binding Motif to Regulate Endosomal Clathrin Dynamics.
Xhabija B, Vacratsis PO.
J Biol Chem 290(35):21676-89. doi: 10.1074/jbc.M115.644757. Epub 2015 Jul 1. 2015
7DNAJC13, PARK21
Clinical, positron emission tomography, and pathological studies of DNAJC13 p.N855S Parkinsonism.
Appel-Cresswell S, Rajput AH, Sossi V, Thompson C, Silva V, McKenzie J, Dinelle K, McCormick SE, Vilariño-Güell C, Stoessl AJ, Dickson DW, Robinson CA, Farrer MJ, Rajput A.
Mov Disord 29(13):1684-7. doi: 10.1002/mds.26019. Epub 2014 Sep 3. 2014
8DNAJC13, PARK21
DNAJC13 mutations in Parkinson disease.
Vilariño-Güell C, Rajput A, Milnerwood AJ, Shah B, Szu-Tu C, Trinh J, Yu I, Encarnacion M, Munsie LN, Tapia L, Gustavsson EK, Chou P, Tatarnikov I, Evans DM, Pishotta FT, Volta M, Beccano-Kelly D, Thompson C, Lin MK, Sherman HE, Han HJ, Guenther BL, Wasserman WW, Bernard V, Ross CJ, Appel-Cresswell S, Stoessl AJ, Robinson CA, Dickson DW, Ross OA, Wszolek ZK, Aasly JO, Wu RM, Hentati F, Gibson RA, McPherson PS, Girard M, Rajput M, Rajput AH, Farrer MJ.
Hum Mol Genet 23(7):1794-801. doi: 10.1093/hmg/ddt570. Epub 2013 Nov 11. 2014
9DNAJC13
RME-8 coordinates the activity of the WASH complex with the function of the retromer SNX dimer to control endosomal tubulation.
Freeman CL, Hesketh G, Seaman MN.
J Cell Sci 127(Pt 9):2053-70. doi: 10.1242/jcs.144659. Epub 2014 Mar 18. 2014
10DNAJC13, MTMR2
Receptor mediated endocytosis 8 is a novel PI(3)P binding protein regulated by myotubularin-related 2.
Xhabija B, Taylor GS, Fujibayashi A, Sekiguchi K, Vacratsis PO.
FEBS Lett 585(12):1722-8. doi: 10.1016/j.febslet.2011.04.016. Epub 2011 Apr 15. 2011
11DNAJC13, HSPA8
RME-8 regulates trafficking of the epidermal growth factor receptor.
Girard M, McPherson PS.
FEBS Lett 582(6):961-6. Epub 2008 Feb 26. 2008
12DNAJC13
Human RME-8 is involved in membrane trafficking through early endosomes.
Fujibayashi A, Taguchi T, Misaki R, Ohtani M, Dohmae N, Takio K, Yamada M, Gu J, Yamakami M, Fukuda M, Waguri S, Uchiyama Y, Yoshimori T, Sekiguchi K.
Cell Struct Funct 33(1):35-50. Epub 2008 Feb 6. 2008
13DNAJC13
The DnaJ-domain protein RME-8 functions in endosomal trafficking.
Girard M, Poupon V, Blondeau F, McPherson PS.
J Biol Chem 280(48):40135-43. Epub 2005 Sep 22. 2005
14DNAJC13
The J-domain protein Rme-8 interacts with Hsc70 to control clathrin-dependent endocytosis in Drosophila.
Chang HC, Hull M, Mellman I.
J Cell Biol 164(7):1055-64. 2004
15DNAJC13, NPHP3, SLSN3
Candidate gene analysis of KIAA0678 encoding a DnaJ-like protein for adolescent nephronophthisis and Senior-Loken syndrome type 3.
Volz A, Melkaoui R, Hildebrandt F, Omran H.
Cytogenet Genome Res 97(3-4):163-6. 2002
16AATK, 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