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 Vivi Li + 382 word(s) 382 2020-12-15 07:53:48

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.
Li, V. FREM1 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5595 (accessed on 21 September 2026).
Li V. FREM1 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5595. Accessed September 21, 2026.
Li, Vivi. "FREM1 Gene" Encyclopedia, https://encyclopedia.pub/entry/5595 (accessed September 21, 2026).
Li, V. (2020, December 25). FREM1 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5595
Li, Vivi. "FREM1 Gene." Encyclopedia. Web. 25 December, 2020.
FREM1 Gene
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/frem1

FRAS1 related extracellular matrix 1

genes

References

  1. Alazami AM, Shaheen R, Alzahrani F, Snape K, Saggar A, Brinkmann B, Bavi P,Al-Gazali LI, Alkuraya FS. FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome. Am J Hum Genet. 2009 Sep;85(3):414-8. doi:10.1016/j.ajhg.2009.08.010. Erratum in: Am J Hum Genet. 2009 Nov;85(5):756.
  2. Pavlakis E, Chiotaki R, Chalepakis G. The role of Fras1/Frem proteins in thestructure and function of basement membrane. Int J Biochem Cell Biol. 2011Apr;43(4):487-95. doi: 10.1016/j.biocel.2010.12.016.
  3. Slavotinek AM, Baranzini SE, Schanze D, Labelle-Dumais C, Short KM, Chao R,Yahyavi M, Bijlsma EK, Chu C, Musone S, Wheatley A, Kwok PY, Marles S, Fryns JP, Maga AM, Hassan MG, Gould DB, Madireddy L, Li C, Cox TC, Smyth I, Chudley AE,Zenker M. Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations inFREM1. J Med Genet. 2011 Jun;48(6):375-82. doi: 10.1136/jmg.2011.089631.
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 : Vivi Li
View Times: 1.0K
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 25 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