| 1 | ANO10, ANO3, ANO5, ANO6
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| Structure and function of TMEM16 proteins (anoctamins).
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| Pedemonte N, Galietta LJ.
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| Physiol Rev 94(2):419-59. doi: 10.1152/physrev.00039.2011. Review.
2014
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| 2 | ANO5, LGMD2L, MMD3
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| Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies.
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| Bolduc V, Marlow G, Boycott KM, Saleki K, Inoue H, Kroon J, Itakura M, Robitaille Y, Parent L, Baas F, Mizuta K, Kamata N, Richard I, Linssen WH, Mahjneh I, de Visser M, Bashir R, Brais B.
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| Am J Hum Genet 86(2):213-21. Epub 2010 Jan 21.PMID: 20096397 2010
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| 3 | ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9
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| Expression and function of epithelial anoctamins.
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| Schreiber R, Uliyakina I, Kongsuphol P, Warth R, Mirza M, Martins JR, Kunzelmann K.
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| J Biol Chem 285(10):7838-45. Epub 2010 Jan 7.PMID: 20056604 2010
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| 4 | ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9, SCAR10
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| Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.
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| Vermeer S, Hoischen A, Meijer RP, Gilissen C, Neveling K, Wieskamp N, de Brouwer A, Koenig M, Anheim M, Assoum M, Drouot N, Todorovic S, Milic-Rasic V, Lochmüller H, Stevanin G, Goizet C, David A, Durr A, Brice A, Kremer B, van de Warrenburg BP, Schijvenaars MM, Heister A, Kwint M, Arts P, van der Wijst J, Veltman J, Kamsteeg EJ, Scheffer H, Knoers N.
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| Am J Hum Genet 87(6):813-9. Epub 2010 Nov 18.PMID: 21092923 2010
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| 5 | ANO5, MMD3
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| A new distal myopathy with mutation in anoctamin 5.
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| Mahjneh I, Jaiswal J, Lamminen A, Somer M, Marlow G, Kiuru-Enari S, Bashir R.
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| Neuromuscul Disord 20(12):791-5. Epub 2010 Aug 7.
2010
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| 6 | ANO2, ANO5
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| Anoctamin/TMEM16 family members are Ca2+-activated Cl- channels.
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| Hartzell HC, Yu K, Xiao Q, Chien LT, Qu Z.
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| J Physiol 587(Pt 10):2127-39. Epub 2008 Nov 17. Review. 2009
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| 7 | ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9, BEST1
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| Bestrophin and TMEM16-Ca(2+) activated Cl(-) channels with different functions.
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| Kunzelmann K, Kongsuphol P, Aldehni F, Tian Y, Ousingsawat J, Warth R, Schreiber R.
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| Cell Calcium 46(4):233-41. Epub 2009 Sep 26. Review.PMID: 19783045 2009
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| 8 | ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9
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| Expression of TMEM16 paralogs during murine embryogenesis.
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| Rock JR, Harfe BD.
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| Dev Dyn 237(9):2566-74.
2008
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| 9 | ANO5, GDD
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| Molecular characterization of GDD1/TMEM16E, the gene product responsible for autosomal dominant gnathodiaphyseal dysplasia.
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| Mizuta K, Tsutsumi S, Inoue H, Sakamoto Y, Miyatake K, Miyawaki K, Noji S, Kamata N, Itakura M.
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| Biochem Biophys Res Commun. 357(1):126-32. Epub 2007 Mar 28. 2007
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| 10 | ANO5, ANO6
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| Identification and characterization of TMEM16E and TMEM16F genes in silico.
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| Katoh M, Katoh M.
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| Int J Oncol 24(5):1345-9. 2004
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| 11 | ANO5, GDD
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| The Novel Gene Encoding a Putative Transmembrane Protein Is Mutated in Gnathodiaphyseal Dysplasia (GDD).
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| Tsutsumi S, Kamata N, Vokes TJ, Maruoka Y, Nakakuki K, Enomoto S, Omura K, Amagasa T, Nagayama M, Saito-Ohara F, Inazawa J, Moritani M, Yamaoka T, Inoue H, Itakura M.
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| Am J Hum Genet 74(6):1255-61. Epub 2004 Apr 29. 2004
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| 12 | ANO1, ANO10, ANO2, ANO3, ANO4, ANO5, ANO6, ANO7, ANO8, ANO9
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| Identification and characterization of TMEM16E and TMEM16F genes in silico.
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| Katoh M, Katoh M.
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| Int J Oncol 24(5):1345-9.
2004
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