CLN3 Gene

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1		Vicky Zhou	+ 590 word(s)	590	2020-12-15 07:47:57

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Zhou, V. CLN3 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5151 (accessed on 25 September 2026).

Zhou V. CLN3 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5151. Accessed September 25, 2026.

Zhou, Vicky. "CLN3 Gene" Encyclopedia, https://encyclopedia.pub/entry/5151 (accessed September 25, 2026).

Zhou, V. (2020, December 24). CLN3 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5151

Zhou, Vicky. "CLN3 Gene." Encyclopedia. Web. 24 December, 2020.

CLN3 Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/cln3

CLN3, battenin

genes

References

Cotman SL, Staropoli JF. The juvenile Batten disease protein, CLN3, and itsrole in regulating anterograde and retrograde post-Golgi trafficking. ClinLipidol. 2012 Feb;7(1):79-91.
Cárcel-Trullols J, Kovács AD, Pearce DA. Cell biology of the NCL proteins:What they do and don't do. Biochim Biophys Acta. 2015 Oct;1852(10 Pt B):2242-55. doi: 10.1016/j.bbadis.2015.04.027.
Kitzmüller C, Haines RL, Codlin S, Cutler DF, Mole SE. A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenileneuronal ceroid lipofuscinosis. Hum Mol Genet. 2008 Jan 15;17(2):303-12.
Ku CA, Hull S, Arno G, Vincent A, Carss K, Kayton R, Weeks D, Anderson GW,Geraets R, Parker C, Pearce DA, Michaelides M, MacLaren RE, Robson AG, Holder GE,Heon E, Raymond FL, Moore AT, Webster AR, Pennesi ME. Detailed Clinical Phenotypeand Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. JAMA Ophthalmol. 2017 Jul 1;135(7):749-760. doi:10.1001/jamaophthalmol.2017.1401.
Mirza M, Vainshtein A, DiRonza A, Chandrachud U, Haslett LJ, Palmieri M,Storch S, Groh J, Dobzinski N, Napolitano G, Schmidtke C, Kerkovich DM. The CLN3 gene and protein: What we know. Mol Genet Genomic Med. 2019 Dec;7(12):e859. doi: 10.1002/mgg3.859.
Oetjen S, Kuhl D, Hermey G. Revisiting the neuronal localization andtrafficking of CLN3 in juvenile neuronal ceroid lipofuscinosis. J Neurochem. 2016Nov;139(3):456-470. doi: 10.1111/jnc.13744.
Phillips SN, Benedict JW, Weimer JM, Pearce DA. CLN3, the protein associatedwith batten disease: structure, function and localization. J Neurosci Res. 2005Mar 1;79(5):573-83. Review.
Rakheja D, Narayan SB, Bennett MJ. The function of CLN3P, the Batten diseaseprotein. Mol Genet Metab. 2008 Mar;93(3):269-74. Review. Erratum in: Mol GenetMetab. 2008 Jun;94(2):270.
Uusi-Rauva K, Kyttälä A, van der Kant R, Vesa J, Tanhuanpää K, Neefjes J,Olkkonen VM, Jalanko A. Neuronal ceroid lipofuscinosis protein CLN3 interactswith motor proteins and modifies location of late endosomal compartments. CellMol Life Sci. 2012 Jun;69(12):2075-89. doi: 10.1007/s00018-011-0913-1.

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Subjects: Genetics & Heredity

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Entry Collection: MedlinePlus

Update Date: 24 Dec 2020

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