Citations for
1FZD2, NXN, RBNS4, RBNS5
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome.
White JJ, Mazzeu JF, Coban-Akdemir Z, Bayram Y, Bahrambeigi V, Hoischen A, van Bon BWM, Gezdirici A, Gulec EY, Ramond F, Touraine R, Thevenon J, Shinawi M, Beaver E, Heeley J, Hoover-Fong J, Durmaz CD, Karabulut HG, Marzioglu-Ozdemir E, Cayir A, Duz MB, Seven M, Price S, Ferreira BM, Vianna-Morgante AM, Ellard S, Parrish A, Stals K, Flores-Daboub J, Jhangiani SN, Gibbs RA; Baylor-Hopkins Center for Mendelian Genomics, Brunner HG, Sutton VR, Lupski JR, Carvalho CMB.
Am J Hum Genet 102(1):27-43. doi: 10.1016/j.ajhg.2017.10.002. Epub 2017 Dec 21. 2018
2FZD2, RBNS4
Nonsense mutations in FZD2 cause autosomal-dominant omodysplasia: Robinow syndrome-like phenotypes.
Nagasaki K, Nishimura G, Kikuchi T, Nyuzuki H, Sasaki S, Ogawa Y, Saitoh A.
Am J Med Genet A m J Med Genet A. 2018 Jan 31. doi: 10.1002/ajmg.a.38623. [Epub ahead of print] 2018
3FZD2
Promotion of epithelial-mesenchymal transition by Frizzled2 is involved in the metastasis of endometrial cancer.
Bian Y, Chang X, Liao Y, Wang J, Li Y, Wang K, Wan X.
Oncol Rep 36(2):803-10. doi: 10.3892/or.2016.4885. Epub 2016 Jun 17. 2016
4FZD2, RBNS4
A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia.
Saal HM, Prows CA, Guerreiro I, Donlin M, Knudson L, Sund KL, Chang CF, Brugmann SA, Stottmann RW.
Hum Mol Genet 24(12):3399-409. doi: 10.1093/hmg/ddv088. Epub 2015 Mar 10. 2015
5FZD2, GATA6, HMGA2
Hmga2 is required for canonical WNT signaling during lung development.
Singh I, Mehta A, Contreras A, Boettger T, Carraro G, Wheeler M, Cabrera-Fuentes HA, Bellusci S, Seeger W, Braun T, Barreto G.
BMC Biol 12:21. doi: 10.1186/1741-7007-12-21. 2014
6FZD2
A noncanonical Frizzled2 pathway regulates epithelial-mesenchymal transition and metastasis.
Gujral TS, Chan M, Peshkin L, Sorger PK, Kirschner MW, MacBeath G.
Cell 159(4):844-56. doi: 10.1016/j.cell.2014.10.032. 2014
7FZD2
Expression of Wnt5a and its receptor Fzd2 is changed in the spinal cord of adult amyotrophic lateral sclerosis transgenic mice.
Li X, Guan Y, Chen Y, Zhang C, Shi C, Zhou F, Yu L, Juan J, Wang X.
Int J Clin Exp Pathol 6(7):1245-60. Print 2013. 2013
8DVL3, FZD2, FZD7, VANGL2
Frizzled 2 and frizzled 7 function redundantly in convergent extension and closure of the ventricular septum and palate: evidence for a network of interacting genes.
Yu H, Ye X, Guo N, Nathans J.
Development 139(23):4383-94. doi: 10.1242/dev.083352. Epub 2012 Oct 24. 2012
9FZD2, WNT5A
Suppression of Frizzled-2-mediated Wnt/CaČ⁺ signaling significantly attenuates intracellular calcium accumulation in vitro and in a rat model of traumatic brain injury.
Niu LJ, Xu RX, Zhang P, Du MX, Jiang XD.
Neuroscience 213:19-28. doi: 10.1016/j.neuroscience.2012.03.057. Epub 2012 Apr 19. 2012
10FZD2, WNT5A
Wnt5a regulates distinct signalling pathways by binding to Frizzled2.
Sato A, Yamamoto H, Sakane H, Koyama H, Kikuchi A.
EMBO J 29(1):41-54. Epub 2009 Nov 12.PMID: 19910923 2010
11FZD1, FZD2
Frizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processes.
Yu H, Smallwood PM, Wang Y, Vidaltamayo R, Reed R, Nathans J.
Development 137(21):3707-17. doi: 10.1242/dev.052001. 2010
12FZD2, ROR2
Ror2 modulates the canonical Wnt signaling in lung epithelial cells through cooperation with Fzd2.
Li C, Chen H, Hu L, Xing Y, Sasaki T, Villosis MF, Li J, Nishita M, Minami Y, Minoo P.
BMC Mol Biol 9:11. doi: 10.1186/1471-2199-9-11. 2008
13FZD1, FZD2
Subcellular localization of frizzled receptors, mediated by their cytoplasmic tails, regulates signaling pathway specificity.
Wu J, Klein TJ, Mlodzik M.
PLoS Biol 2(7):E158. Epub 2004 Jul 13. 2004
14FZD2, ROR2
The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway.
Oishi I, Suzuki H, Onishi N, Takada R, Kani S, Ohkawara B, Koshida I, Suzuki K, Yamada G, Schwabe GC, Mundlos S, Shibuya H, Takada S, Minami Y.
Genes Cells 8(7):645-54. 2003
15FZD1, FZD2, FZD7
Molecular cloning, differential expression, and chromosomal localization of human frizzled-1, frizzled-2, and frizzled-7.
Sagara N, et al.
Biochem Biophys Res Commun 252 : 117-122. 1998
16FZD2, FZD9, SFRP1, SFRP2, FZD8
A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled.
Wang Y, Macke JP, Abella BS, Andreasson K, Worley P, Gilbert DJ, Copeland NG, Jenkins NA, Nathans J.
J Biol Chem 271(8):4468-76. 1996
17FZD2
A human homologue of the Drosophila polarity gene frizzled has been identified and mapped to 17q21.1.
Zhao Z, et al.
Genomics 27 : 370-373. 1995