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Zhou, V. AMN Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4671 (accessed on 23 October 2026).
Zhou V. AMN Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4671. Accessed October 23, 2026.
Zhou, Vicky. "AMN Gene" Encyclopedia, https://encyclopedia.pub/entry/4671 (accessed October 23, 2026).
Zhou, V. (2020, December 24). AMN Gene. In Encyclopedia. https://encyclopedia.pub/entry/4671
Zhou, Vicky. "AMN Gene." Encyclopedia. Web. 24 December, 2020.

AMN Gene

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

amnion associated transmembrane protein

genes

References

  1. Beech CM, Liyanarachchi S, Shah NP, Sturm AC, Sadiq MF, de la Chapelle A,Tanner SM. Ancient founder mutation is responsible for Imerslund-GräsbeckSyndrome among diverse ethnicities. Orphanet J Rare Dis. 2011 Nov 13;6:74. doi:10.1186/1750-1172-6-74.
  2. Fyfe JC, Madsen M, Højrup P, Christensen EI, Tanner SM, de la Chapelle A, HeQ, Moestrup SK. The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. Blood. 2004 Mar 1;103(5):1573-9.
  3. Kozyraki R, Cases O. Vitamin B12 absorption: mammalian physiology and acquiredand inherited disorders. Biochimie. 2013 May;95(5):1002-7. doi:10.1016/j.biochi.2012.11.004.
  4. Namour F, Dobrovoljski G, Chery C, Audonnet S, Feillet F, Sperl W, Gueant JL. Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome withcompound AMN mutations in intron 3 and exon 7. Haematologica. 2011Nov;96(11):1715-9. doi: 10.3324/haematol.2011.043984.
  5. Watkins D, Rosenblatt DS. Lessons in biology from patients with inborn errors of vitamin B12 metabolism. Biochimie. 2013 May;95(5):1019-22. doi:10.1016/j.biochi.2013.01.013.
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Update Date: 24 Dec 2020
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