lebercilin-like protein isoform X1 [Homo sapiens]

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Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. [Nat Genet. 2007]
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
den Hollander AI, Koenekoop RK, Mohamed MD, Arts HH, Boldt K, Towns KV, Sedmak T, Beer M, Nagel-Wolfrum K, McKibbin M, et al. Nat Genet. 2007 Jul; 39(7):889-95. Epub 2007 Jun 3.
Trisomy 21 Alters DNA Methylation in Parent-of-Origin-Dependent and -Independent Manners. [PLoS One. 2016]
Trisomy 21 Alters DNA Methylation in Parent-of-Origin-Dependent and -Independent Manners.
Alves da Silva AF, Machado FB, Pavarino ÉC, Biselli-Périco JM, Zampieri BL, da Silva Francisco Junior R, Mozer Rodrigues PT, Terra Machado D, Santos-Rebouças CB, Gomes Fernandes M, et al. PLoS One. 2016; 11(4):e0154108. Epub 2016 Apr 21.
The palmitoyl acyltransferase HIP14 shares a high proportion of interactors with huntingtin: implications for a role in the pathogenesis of Huntington's disease. [Hum Mol Genet. 2014]
The palmitoyl acyltransferase HIP14 shares a high proportion of interactors with huntingtin: implications for a role in the pathogenesis of Huntington's disease.
Butland SL, Sanders SS, Schmidt ME, Riechers SP, Lin DT, Martin DD, Vaid K, Graham RK, Singaraja RR, Wanker EE, et al. Hum Mol Genet. 2014 Aug 1; 23(15):4142-60. Epub 2014 Apr 4.

RefSeq mRNA
See reference mRNA sequence for the LCA5L gene (XM_011529460.2).
RefSeq protein isoforms
See 84 reference sequence protein isoforms for the LCA5L gene.

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Protein