AMT Gene

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Zhou, V. AMT Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4673 (accessed on 28 September 2026).

Zhou V. AMT Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4673. Accessed September 28, 2026.

Zhou, Vicky. "AMT Gene" Encyclopedia, https://encyclopedia.pub/entry/4673 (accessed September 28, 2026).

Zhou, V. (2020, December 24). AMT Gene. In Encyclopedia. https://encyclopedia.pub/entry/4673

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

AMT Gene

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

aminomethyltransferase

genes

References

Coughlin CR 2nd, Swanson MA, Kronquist K, Acquaviva C, Hutchin T,Rodríguez-Pombo P, Väisänen ML, Spector E, Creadon-Swindell G, Brás-Goldberg AM, Rahikkala E, Moilanen JS, Mahieu V, Matthijs G, Bravo-Alonso I, Pérez-Cerdá C,Ugarte M, Vianey-Saban C, Scharer GH, Van Hove JL. The genetic basis of classicnonketotic hyperglycinemia due to mutations in GLDC and AMT. Genet Med. 2017Jan;19(1):104-111. doi: 10.1038/gim.2016.74.Med. 2018 Jan 04;:.
Kikuchi G, Motokawa Y, Yoshida T, Hiraga K. Glycine cleavage system: reaction mechanism, physiological significance, and hyperglycinemia. Proc Jpn Acad Ser BPhys Biol Sci. 2008;84(7):246-63. Review.
Kure S, Kato K, Dinopoulos A, Gail C, DeGrauw TJ, Christodoulou J, Bzduch V,Kalmanchey R, Fekete G, Trojovsky A, Plecko B, Breningstall G, Tohyama J, Aoki Y,Matsubara Y. Comprehensive mutation analysis of GLDC, AMT, and GCSH in nonketotichyperglycinemia. Hum Mutat. 2006 Apr;27(4):343-52.
Okamura-Ikeda K, Hosaka H, Yoshimura M, Yamashita E, Toma S, Nakagawa A,Fujiwara K, Motokawa Y, Taniguchi H. Crystal structure of human T-protein ofglycine cleavage system at 2.0 A resolution and its implication for understandingnon-ketotic hyperglycinemia. J Mol Biol. 2005 Sep 2;351(5):1146-59.
Swanson MA, Coughlin CR Jr, Scharer GH, Szerlong HJ, Bjoraker KJ, Spector EB, Creadon-Swindell G, Mahieu V, Matthijs G, Hennermann JB, Applegarth DA, Toone JR,Tong S, Williams K, Van Hove JL. Biochemical and molecular predictors forprognosis in nonketotic hyperglycinemia. Ann Neurol. 2015 Oct;78(4):606-18. doi: 10.1002/ana.24485.
Toone JR, Applegarth DA, Levy HL, Coulter-Mackie MB, Lee G. Molecular genetic and potential biochemical characteristics of patients with T-protein deficiencyas a cause of glycine encephalopathy (NKH). Mol Genet Metab. 2003Aug;79(4):272-80.
Van Hove JLK, Coughlin C II, Swanson M, Hennermann JB. NonketoticHyperglycinemia. 2002 Nov 14 [updated 2019 May 23]. In: Adam MP, Ardinger HH,Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020. Availablefrom http://www.ncbi.nlm.nih.gov/books/NBK1357/

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Subjects: Genetics & Heredity

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Update Date: 24 Dec 2020

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