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Li, V. FKBP10 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5531 (accessed on 21 September 2026).
Li V. FKBP10 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5531. Accessed September 21, 2026.
Li, Vivi. "FKBP10 Gene" Encyclopedia, https://encyclopedia.pub/entry/5531 (accessed September 21, 2026).
Li, V. (2020, December 25). FKBP10 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5531
Li, Vivi. "FKBP10 Gene." Encyclopedia. Web. 25 December, 2020.
FKBP10 Gene
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/fkbp10

FKBP prolyl isomerase 10

genes

References

  1. Barnes AM, Cabral WA, Weis M, Makareeva E, Mertz EL, Leikin S, Eyre D,Trujillo C, Marini JC. Absence of FKBP10 in recessive type XI osteogenesisimperfecta leads to diminished collagen cross-linking and reduced collagendeposition in extracellular matrix. Hum Mutat. 2012 Nov;33(11):1589-98. doi:10.1002/humu.22139.
  2. Ishikawa Y, Vranka J, Wirz J, Nagata K, Bächinger HP. The rough endoplasmicreticulum-resident FK506-binding protein FKBP65 is a molecular chaperone thatinteracts with collagens. J Biol Chem. 2008 Nov 14;283(46):31584-90. doi:10.1074/jbc.M802535200.
  3. Miao M, Reichheld SE, Muiznieks LD, Huang Y, Keeley FW. Elastin bindingprotein and FKBP65 modulate in vitro self-assembly of human tropoelastin.Biochemistry. 2013 Nov 5;52(44):7731-41. doi: 10.1021/bi400760f.
  4. Schwarze U, Cundy T, Pyott SM, Christiansen HE, Hegde MR, Bank RA, Pals G,Ankala A, Conneely K, Seaver L, Yandow SM, Raney E, Babovic-Vuksanovic D, Stoler J, Ben-Neriah Z, Segel R, Lieberman S, Siderius L, Al-Aqeel A, Hannibal M,Hudgins L, McPherson E, Clemens M, Sussman MD, Steiner RD, Mahan J, Smith R,Anyane-Yeboa K, Wynn J, Chong K, Uster T, Aftimos S, Sutton VR, Davis EC, Kim LS,Weis MA, Eyre D, Byers PH. Mutations in FKBP10, which result in Bruck syndromeand recessive forms of osteogenesis imperfecta, inhibit the hydroxylation oftelopeptide lysines in bone collagen. Hum Mol Genet. 2013 Jan 1;22(1):1-17. doi: 10.1093/hmg/dds371.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Vivi Li
View Times: 730
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 25 Dec 2020
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