Your browser does not fully support modern features. Please upgrade for a smoother experience.
Submitted Successfully!
Thank you for your contribution! You can also upload a video entry or images related to this topic. For video creation, please contact our Academic Video Service.
Version Summary Created by Modification Content Size Created at Operation
1 Peter Tang + 319 word(s) 319 2020-12-15 08:14:54

Video Upload Options

We provide professional Academic Video Service to translate complex research into visually appealing presentations. Would you like to try it?
No, upload directly Yes
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Tang, P. ZFYVE26 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4651 (accessed on 29 September 2026).
Tang P. ZFYVE26 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4651. Accessed September 29, 2026.
Tang, Peter. "ZFYVE26 Gene" Encyclopedia, https://encyclopedia.pub/entry/4651 (accessed September 29, 2026).
Tang, P. (2020, December 24). ZFYVE26 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4651
Tang, Peter. "ZFYVE26 Gene." Encyclopedia. Web. 24 December, 2020.
ZFYVE26 Gene
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/zfyve26

Zinc finger FYVE-type containing 26: the ZFYVE26 gene provides instructions for making a protein called spastizin.

genes

References

  1. Hanein S, Martin E, Boukhris A, Byrne P, Goizet C, Hamri A, Benomar A, Lossos A, Denora P, Fernandez J, Elleuch N, Forlani S, Durr A, Feki I, Hutchinson M,Santorelli FM, Mhiri C, Brice A, Stevanin G. Identification of the SPG15 gene,encoding spastizin, as a frequent cause of complicated autosomal-recessivespastic paraplegia, including Kjellin syndrome. Am J Hum Genet. 2008Apr;82(4):992-1002. doi: 10.1016/j.ajhg.2008.03.004.
  2. Vantaggiato C, Clementi E, Bassi MT. ZFYVE26/SPASTIZIN: a close link betweencomplicated hereditary spastic paraparesis and autophagy. Autophagy. 2014Feb;10(2):374-5. doi: 10.4161/auto.27173.
  3. Vantaggiato C, Crimella C, Airoldi G, Polishchuk R, Bonato S, Brighina E,Scarlato M, Musumeci O, Toscano A, Martinuzzi A, Santorelli FM, Ballabio A,Bresolin N, Clementi E, Bassi MT. Defective autophagy in spastizin mutatedpatients with hereditary spastic paraparesis type 15. Brain. 2013 Oct;136(Pt10):3119-39. doi: 10.1093/brain/awt227.
More
©Text is available under the terms and conditions of the Creative Commons-Attribution ShareAlike (CC BY-SA) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
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 : Peter Tang
View Times: 682
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 24 Dec 2020
Table of Contents
    Notice
    You are not a member of the advisory board for this topic. If you want to update advisory board member profile, please contact office@encyclopedia.pub.
    OK
    Confirm
    Only members of the Encyclopedia advisory board for this topic are allowed to note entries. Would you like to become an advisory board member of the Encyclopedia?
    Yes
    No
    ${ textCharacter }/${ maxCharacter }
    Submit
    Cancel
    There is no comment~
    ${ textCharacter }/${ maxCharacter }
    Submit
    Cancel
    ${ selectedItem.replyTextCharacter }/${ selectedItem.replyMaxCharacter }
    Submit
    Cancel
    Confirm
    Are you sure to Delete?
    Yes No
    Academic Video Service
    Feedback