1 | ADGRV1, DNAH5
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| A novel role for ciliary function in atopy: ADGRV1 and DNAH5 interactions.
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| Sugier PE, Brossard M, Sarnowski C, Vaysse A, Morin A, Pain L, Margaritte-Jeannin P, Dizier MH, Cookson WOCM, Lathrop M, Moffatt MF, Laprise C, Demenais F, Bouzigon E.
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| J Allergy Clin Immunol 141(5):1659-1667.e11. doi: 10.1016/j.jaci.2017.06.050. Epub 2017 Sep 18.
2018
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2 | ADGRV1, PDZD7, USH1C, USH2A, WHRN
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| The roles of USH1 proteins and PDZ domain-containing USH proteins in USH2 complex integrity in cochlear hair cells.
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| Zou J, Chen Q, Almishaal A, Mathur PD, Zheng T, Tian C, Zheng QY, Yang J.
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| Hum Mol Genet 26(3):624-636. doi: 10.1093/hmg/ddw421.
2017
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3 | ADGRV1, USH2C
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| USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms.
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| Moteki H, Yoshimura H, Azaiez H, Booth KT, Shearer AE, Sloan CM, Kolbe DL, Murata T, Smith RJ, Usami S.
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| Ann Otol Rhinol Laryngol 124 Suppl 1:123S-8S. doi: 10.1177/0003489415574070. Epub 2015 Mar 5.
2015
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4 | ADGRV1, CLRN1
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| Domain analyses of Usher syndrome causing Clarin-1 and GPR98 protein models.
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| Khan SH, Javed MR, Qasim M, Shahzadi S, Jalil A, Rehman SU.
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| Bioinformation 10(8):491-5. doi: 10.6026/97320630010491. eCollection 2014.
2014
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5 | ADGRV1, PDZD7
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| Constitutive Gαi coupling activity of very large G protein-coupled receptor 1 (VLGR1) and its regulation by PDZD7 protein.
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| Hu QX, Dong JH, Du HB, Zhang DL, Ren HZ, Ma ML, Cai Y, Zhao TC, Yin XL, Yu X, Xue T, Xu ZG, Sun JP.
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| J Biol Chem 289(35):24215-25. doi: 10.1074/jbc.M114.549816. Epub 2014 Jun 24.
2014
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6 | ADGRV1, MAG
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| Very large G protein-coupled receptor 1 regulates myelin-associated glycoprotein via Gαs/Gαq-mediated protein kinases A/C.
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| Shin D, Lin ST, Fu YH, Ptácek LJ.
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| Proc Natl Acad Sci U S A 110(47):19101-6. doi: 10.1073/pnas.1318501110. Epub 2013 Nov 4.
2013
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7 | ADGRV1, USH2C, WHRN
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| The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.
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| García-García G, Besnard T, Baux D, Vaché C, Aller E, Malcolm S, Claustres M, Millan JM, Roux AF.
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| Mol Vis 19:367-73. Epub 2013 Feb 13. 2013
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8 | ADGRV1
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| The very large G protein coupled receptor (Vlgr1) in hair cells.
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| Sun JP, Li R, Ren HZ, Xu AT, Yu X, Xu ZG.
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| J Mol Neurosci 50(1):204-14. doi: 10.1007/s12031-012-9911-5. Epub 2012 Nov 20. Review.
2013
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9 | ADGRV1, SNAP25
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| Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cells.
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| Zallocchi M, Delimont D, Meehan DT, Cosgrove D.
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| J Neurosci 32(40):13841-59. doi: 10.1523/JNEUROSCI.1242-12.2012.
2012
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10 | ADGRV1
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| GPR98/Gpr98 gene is involved in the regulation of human and mouse bone mineral density.
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| Urano T, Shiraki M, Yagi H, Ito M, Sasaki N, Sato M, Ouchi Y, Inoue S.
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| J Clin Endocrinol Metab 97(4):E565-74. doi: 10.1210/jc.2011-2393. Epub 2012 Mar 14.
2012
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11 | ADGRV1, CDH23, CLRN1, PCDH15
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| Role for a novel Usher protein complex in hair cell synaptic maturation.
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| Zallocchi M, Meehan DT, Delimont D, Rutledge J, Gratton MA, Flannery J, Cosgrove D.
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| PLoS One 7(2):e30573. doi: 10.1371/journal.pone.0030573. Epub 2012 Feb 17.
2012
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12 | ADGRV1, CDH23, CLRN1, MYO7A, PCDH15, USH1B, USH1C, USH1D, USH1F, USH1G, USH2A, USH2C, USH2D, USH3A, WHRN
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| Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells.
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| Zallocchi M, Sisson JH, Cosgrove D.
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| Biochemistry 49(6):1236-47.PMID: 20058854 2010
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13 | ADGRV1, USH2A, USH2C, USH2D, WHRN
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| An USH2A founder mutation is the major cause of Usher syndrome type 2 in Canadians of French origin and confirms common roots of Quebecois and Acadians.
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| Ebermann I, Koenekoop RK, Lopez I, Bou-Khzam L, Pigeon R, Bolz HJ.
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| Eur J Hum Genet 17(1):80-4. Epub 2008 Jul 30. 2009
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14 | ADGRV1, USH2C
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| A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family.
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| Hilgert N, Kahrizi K, Dieltjens N, Bazazzadegan N, Najmabadi H, Smith RJ, Van Camp G.
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| J Med Genet 46(4):272-6. 2009
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15 | ADGRV1, USH2C
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| GPR98 mutations cause Usher syndrome type 2 in males.
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| Ebermann I, Wiesen MH, Zrenner E, Lopez I, Pigeon R, Kohl S, Löwenheim H, Koenekoop RK, Bolz HJ.
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| J Med Genet 46(4):277-80. 2009
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16 | ADGRV1, PDE6B
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| Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
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| Hmani-Aifa M, Benzina Z, Zulfiqar F, Dhouib H, Shahzadi A, Ghorbel A, Rebaï A, Söderkvist P, Riazuddin S, Kimberling WJ, Ayadi H.
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| Eur J Hum Genet 17(4):474-82. Epub 2008 Oct 15. 2009
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17 | ADGRV1, CETN3, DEL5Q14, LYSMD3, POLR3G
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| A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients.
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| Engels H, Wohlleber E, Zink A, Hoyer J, Ludwig KU, Brockschmidt FF, Wieczorek D, Moog U, Hellmann-Mersch B, Weber RG, Willatt L, Kreiss-Nachtsheim M, Firth HV, Rauch A.
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| Eur J Hum Genet 17(12):1592-9. Epub 2009 May 27. 2009
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18 | ADGRV1, MYO7A, USH1G, VEZT, WHRN
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| A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells.
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| Maerker T, van Wijk E, Overlack N, Kersten FF, McGee J, Goldmann T, Sehn E, Roepman R, Walsh EJ, Kremer H, Wolfrum U.
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| Hum Mol Genet 17(1):71-86. Epub 2007 Sep 28. 2008
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19 | ADGRV1, MYO7A, PCDH15, USH1B, USH1F, USH2A, USH2C
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| Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
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| Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Roman AJ, Gardner LM, Prosser HM, Mishra M, Bech-Hansen NT, Herrera W, Schwartz SB, Liu XZ, Kimberling WJ, Steel KP, Williams DS.
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| Hum Mol Genet 17(15):2405-15. Epub 2008 May 7. 2008
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20 | ADGRV1, USH2A, VEZT, WHRN
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| Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning.
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| Michalski N, Michel V, Bahloul A, Lefèvre G, Barral J, Yagi H, Chardenoux S, Weil D, Martin P, Hardelin JP, Sato M, Petit C.
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| J Neurosci 27(24):6478-88. 2007
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21 | ADGRV1, USH2A, WHRN
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| The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1.
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| van Wijk E, van der Zwaag B, Peters T, Zimmermann U, Te Brinke H, Kersten FF, Marker T, Aller E, Hoefsloot LH, Cremers CW, Cremers FP, Wolfrum U, Knipper M, Roepman R, Kremer H.
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| Hum Mol Genet 15(5):751-65. Epub 2006 Jan 24. 2006
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22 | ADGRV1, CDH23, CLRN1, MYO7A, PCDH15, USH1B, USH1C, USH1D, USH1F, USH2B, USH2C
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| First evidence for a molecular link between Usher 1 and Usher 2 syndromes.
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| Stein R.
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| Clin Genet 69(6):483-485. No abstract available. 2006
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23 | ADGRV1, USH1C
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| The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.
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| Johnson KR, Zheng QY, Weston MD, Ptacek LJ, Noben-Trauth K.
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| Genomics 85(5):582-90. 2005
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24 | ADGRV1, SLC4A7, USH1C, USH2A
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| Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2.
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| Reiners J, van Wijk E, Marker T, Zimmermann U, Jurgens K, te Brinke H, Overlack N, Roepman R, Knipper M, Kremer H, Wolfrum U.
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| Hum Mol Genet 14(24):3933-43. Epub 2005 Nov 21. 2005
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25 | ADGRV1, USH2A, USH2C
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| Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype.
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| Schwartz SB, Aleman TS, Cideciyan AV, Windsor EA, Sumaroka A, Roman AJ, Rane T, Smilko EE, Bennett J, Stone EM, Kimberling WJ, Liu XZ, Jacobson SG.
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| Invest Ophthalmol Vis Sci 46(2):734-43. 2005
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26 | ADGRV1, USH2C
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| Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II.
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| Weston MD, Luijendijk MW, Humphrey KD, Moller C, Kimberling WJ.
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| Am J Hum Genet 74(2):357-66. Epub 2004 Jan 20. 2004
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27 | ADGRA3, ADGRB1, ADGRB2, ADGRB3, ADGRG1, ADGRG2, ADGRG6, ADGRL1, ADGRL2, ADGRL3, ADGRL4, ADGRV1, CD97, EMR3, GPR110, GPR111, GPR114, GPR115, GPR116, GPR124, GPR133, GPR144, GPR97
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| The human and mouse repertoire of the adhesion family of G-protein-coupled receptors.
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| Bjarnadottir TK, Fredriksson R, Hoglund PJ, Gloriam DE, Lagerstrom MC, Schioth HB.
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| Genomics 84(1):23-33. 2004
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28 | ADGRV1
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| Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system.
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| McMillan DR, Kayes-Wandover KM, Richardson JA, White PC.
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| J Biol Chem 277(1):785-92. 2002
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29 | ADGRV1, FEB4
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| A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures.
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| Nakayama J, Fu YH, Clark AM, Nakahara S, Hamano K, Iwasaki N, Matsui A, Arinami T, Ptacek LJ.
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| Ann Neurol 52(5):654-7. 2002
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30 | ADGRV1, LGI1, LGI2, LGI3, LGI4, TSPEAR
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| A common protein interaction domain links two recently identified epilepsy genes.
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| Scheel H, Tomiuk S, Hofmann K.
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| Hum Mol Genet 11(15):1757-62. 2002
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31 | ADGRV1, FEB4
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| A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures.
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| Nakayama J, Fu YH, Clark AM, Nakahara S, Hamano K, Iwasaki N, Matsui A, Arinami T, Ptácek LJ.
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| Ann Neurol 52(5):654-7.
2002
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32 | ADGRV1
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| A novel gene causing a mendelian audiogenic mouse epilepsy.
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| Skradski SL, Clark AM, Jiang H, White HS, Fu YH, Ptacek LJ.
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| Neuron 31(4):537-44. 2001
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33 | ADGRV1
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| Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain.
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| Nikkila H, McMillan DR, Nunez BS, Pascoe L, Curnow KM, White PC.
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| Mol Endocrinol 14(9):1351-64. 2000
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34 | ADGRV1
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| Structural requirements for alpha-latrotoxin binding and alpha-latrotoxin-stimulated secretion. A study with calcium-independent receptor of alpha-latrotoxin (cirl) deletion mutants.
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| Krasnoperov V, et al.
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| J Biol Chem 274 : 3590-3596. 1999
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35 | ADGRV1, LPHN2
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| The latrophilin family: multiply spliced G protein-coupled receptors with differential tissue distribution.
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| Matsushita H, et al.
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| FEBS Lett 443(3):348-52. 1999
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36 | ADGRV1
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| Ca2+-independent insulin exocytosis induced by alpha-latrotoxin requires latrophilin, a G protein-coupled receptor.
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| Lang J, et al.
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| EMBO J 17 : 648-657. 1998
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37 | ADGRV1, NRXN1
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| Alpha-Latrotoxin receptor CIRL/latrophilin 1 (CL1) defines an unusual family of ubiquitous G-protein-linked receptors. G-protein coupling not required for triggering exocytosis.
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| Sugita S, et al.
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| J Biol Chem 273 : 32715-32724. 1998
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38 | AATK, 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
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| 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.
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| Ishikawa K, Nagase T, Suyama M, Miyajima N, Tanaka A, Kotani H, Nomura N,Ohara O.
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| DNA Res 5(3):169-76. 1998
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39 | ADGRV1
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| Alpha-latrotoxin receptor, latrophilin, is a novel member of the secretin family of G protein-coupled receptors.
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| Lelianova VG, et al.
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| J Biol Chem 272 : 21504-21508. 1997
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