Frizzled homolog 4 (Drosophila), also known as FZD4, is a human gene.cite web | title = Entrez Gene: FZD4 frizzled homolog 4 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8322| accessdate = ] FZD4 has also been designated as CD344 (cluster of differentiation 344).

section_title =
summary_text = This gene is a member of the frizzled gene family. Members of this family encode seven-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins. Most frizzled receptors are coupled to the beta-catenin canonical signaling pathway. This protein may play a role as a positive regulator of the Wingless type MMTV integration site signaling pathway. A transcript variant retaining intronic sequence and encoding a shorter isoform has been described, however, its expression is not supported by other experimental evidence.cite web | title = Entrez Gene: FZD4 frizzled homolog 4 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8322| accessdate = ]

ee also

* Frizzled


Further reading

citations =
*cite journal | author=Li Y, Fuhrmann C, Schwinger E, "et al." |title=The gene for autosomal dominant familial exudative vitreoretinopathy (Criswick-Schepens) on the long arm of chromosome 11. |journal=Am. J. Ophthalmol. |volume=113 |issue= 6 |pages= 712–3 |year= 1992 |pmid= 1598965 |doi=
*cite journal | author=Tanaka S, Akiyoshi T, Mori M, "et al." |title=A novel frizzled gene identified in human esophageal carcinoma mediates APC/beta-catenin signals. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 17 |pages= 10164–9 |year= 1998 |pmid= 9707618 |doi=
*cite journal | author=Kirikoshi H, Sagara N, Koike J, "et al." |title=Molecular cloning and characterization of human Frizzled-4 on chromosome 11q14-q21. |journal=Biochem. Biophys. Res. Commun. |volume=264 |issue= 3 |pages= 955–61 |year= 1999 |pmid= 10544037 |doi= 10.1006/bbrc.1999.1612
*cite journal | author=Sagara N, Kirikoshi H, Terasaki H, "et al." |title=FZD4S, a splicing variant of frizzled-4, encodes a soluble-type positive regulator of the WNT signaling pathway. |journal=Biochem. Biophys. Res. Commun. |volume=282 |issue= 3 |pages= 750–6 |year= 2001 |pmid= 11401527 |doi= 10.1006/bbrc.2001.4634
*cite journal | author=Takeda S, Kadowaki S, Haga T, "et al." |title=Identification of G protein-coupled receptor genes from the human genome sequence. |journal=FEBS Lett. |volume=520 |issue= 1-3 |pages= 97–101 |year= 2002 |pmid= 12044878 |doi=
*cite journal | author=Hering H, Sheng M |title=Direct interaction of Frizzled-1, -2, -4, and -7 with PDZ domains of PSD-95. |journal=FEBS Lett. |volume=521 |issue= 1-3 |pages= 185–9 |year= 2002 |pmid= 12067714 |doi=
*cite journal | author=Robitaille J, MacDonald ML, Kaykas A, "et al." |title=Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy. |journal=Nat. Genet. |volume=32 |issue= 2 |pages= 326–30 |year= 2002 |pmid= 12172548 |doi= 10.1038/ng957
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Chen W, ten Berge D, Brown J, "et al." |title=Dishevelled 2 recruits beta-arrestin 2 to mediate Wnt5A-stimulated endocytosis of Frizzled 4. |journal=Science |volume=301 |issue= 5638 |pages= 1391–4 |year= 2003 |pmid= 12958364 |doi= 10.1126/science.1082808
*cite journal | author=Toomes C, Downey LM, Bottomley HM, "et al." |title=Identification of a fourth locus (EVR4) for familial exudative vitreoretinopathy (FEVR). |journal=Mol. Vis. |volume=10 |issue= |pages= 37–42 |year= 2004 |pmid= 14737064 |doi=
*cite journal | author=Toomes C, Bottomley HM, Jackson RM, "et al." |title=Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. |journal=Am. J. Hum. Genet. |volume=74 |issue= 4 |pages= 721–30 |year= 2004 |pmid= 15024691 |doi= 10.1086/383202
*cite journal | author=Yao R, Natsume Y, Noda T |title=MAGI-3 is involved in the regulation of the JNK signaling pathway as a scaffold protein for frizzled and Ltap. |journal=Oncogene |volume=23 |issue= 36 |pages= 6023–30 |year= 2005 |pmid= 15195140 |doi= 10.1038/sj.onc.1207817
*cite journal | author=Toomes C, Bottomley HM, Scott S, "et al." |title=Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy. |journal=Invest. Ophthalmol. Vis. Sci. |volume=45 |issue= 7 |pages= 2083–90 |year= 2004 |pmid= 15223780 |doi=
*cite journal | author=Omoto S, Hayashi T, Kitahara K, "et al." |title=Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with FZD4 mutations (H69Y and C181R). |journal=Ophthalmic Genet. |volume=25 |issue= 2 |pages= 81–90 |year= 2004 |pmid= 15370539 |doi= 10.1080/13816810490514270
*cite journal | author=Yoshida S, Arita R, Yoshida A, "et al." |title=Novel mutation in FZD4 gene in a Japanese pedigree with familial exudative vitreoretinopathy. |journal=Am. J. Ophthalmol. |volume=138 |issue= 4 |pages= 670–1 |year= 2004 |pmid= 15488808 |doi= 10.1016/j.ajo.2004.05.001
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Qin M, Hayashi H, Oshima K, "et al." |title=Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes. |journal=Hum. Mutat. |volume=26 |issue= 2 |pages= 104–12 |year= 2006 |pmid= 15981244 |doi= 10.1002/humu.20191
*cite journal | author=Nallathambi J, Shukla D, Rajendran A, "et al." |title=Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy. |journal=Mol. Vis. |volume=12 |issue= |pages= 1086–92 |year= 2006 |pmid= 17093393 |doi=
*cite journal | author=Planutis K, Planutiene M, Moyer MP, "et al." |title=Regulation of norrin receptor frizzled-4 by Wnt2 in colon-derived cells. |journal=BMC Cell Biol. |volume=8 |issue= |pages= 12 |year= 2007 |pmid= 17386109 |doi= 10.1186/1471-2121-8-12

update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes

Wikimedia Foundation. 2010.

Игры ⚽ Нужно сделать НИР?

Look at other dictionaries:

  • Frizzled — Pfam box Symbol = Frizzled Name = Frizzled/Smoothened family membrane region width = caption = Pfam= PF01534 InterPro= IPR000539 SMART= PROSITE = PDOC50038 SCOP = TCDB = OPM family= OPM protein= PDB=Frizzled is a family of G protein coupled… …   Wikipedia

  • Genetic disorder — For a non technical introduction to the topic, see Introduction to genetics. Genetic disorder Classification and external resources MeSH D030342 A genetic disorder is an illness caused by abnormalities in genes or …   Wikipedia

  • Achondroplasia — Classification and external resources Jason Acuña, alias Wee Man , a star of Jackass …   Wikipedia

  • Donohue syndrome — Classification and external resources insulin receptor OMIM 246200 …   Wikipedia

  • Hirschsprung's disease — Classification and external resources Histopathology of Hirschsprung disease. Enzyme histochemistry showing aberrant acetylcholine esterase (ACHE) positive fibres (brown) in the lamina propria mucosae …   Wikipedia

  • Congenital hypothyroidism — Classification and external resources ICD 10 E00, E03.0, E03.1 …   Wikipedia

  • Osteopetrosis — (Malignant) Classification and external resources X ray of the pelvis of a patient with osteopetrosis, adult onset form (Albers Schonberg disease). Note the dense bones. ICD …   Wikipedia

  • Hereditary hemorrhagic telangiectasia — Classification and external resources Characteristic lip telangiectases. ICD 10 I …   Wikipedia

  • Congenital insensitivity to pain with anhidrosis — Classification and external resources OMIM 256800 DiseasesDB 32097 MeSH …   Wikipedia

  • Crouzon syndrome — Classification and external resources ICD 10 Q75.1 ICD 9 756.0 …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”