MFRP
{{Short description|Protein-coding gene in the species Homo sapiens}}
{{Infobox_gene}}
Membrane frizzled-related protein is a protein that in humans is encoded by the MFRP gene.{{cite journal | author = Katoh M | title = Molecular cloning and characterization of MFRP, a novel gene encoding a membrane-type Frizzled-related protein | journal = Biochem Biophys Res Commun | volume = 282 | issue = 1 | pages = 116–23 |date=Mar 2001 | pmid = 11263980 | doi = 10.1006/bbrc.2001.4551 }}{{cite web | title = Entrez Gene: MFRP membrane frizzled-related protein| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=83552}}
References
{{reflist}}
Further reading
{{refbegin | 2}}
- {{cite journal |vauthors=Metlapally R, Li YJ, Tran-Viet KN, etal |title=Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia. |journal=Mol. Vis. |volume=14 |pages= 387–93 |year= 2008|pmid= 18334955 | pmc=2268852 }}
- {{cite journal |vauthors=Ayala-Ramirez R, Graue-Wiechers F, Robredo V, etal |title=A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation. |journal=Mol. Vis. |volume=12 |pages= 1483–9 |year= 2007 |pmid= 17167404 }}
- {{cite journal |vauthors=Yang L, Yamasaki K, Shirakata Y, etal |title=Bone morphogenetic protein-2 modulates Wnt and frizzled expression and enhances the canonical pathway of Wnt signaling in normal keratinocytes. |journal=J. Dermatol. Sci. |volume=42 |issue= 2 |pages= 111–9 |year= 2006 |pmid= 16442268 |doi= 10.1016/j.jdermsci.2005.12.011 }}
- {{cite journal |vauthors=Pauer GJ, Xi Q, Zhang K, etal |title=Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations. |journal=Ophthalmic Genet. |volume=26 |issue= 4 |pages= 157–61 |year= 2006 |pmid= 16352475 |doi= 10.1080/13816810500374425 |s2cid=43634962 }}
- {{cite journal |vauthors=Mandal MN, Heckenlively JR, Burch T, etal |title=Sequencing arrays for screening multiple genes associated with early-onset human retinal degenerations on a high-throughput platform. |journal=Invest. Ophthalmol. Vis. Sci. |volume=46 |issue= 9 |pages= 3355–62 |year= 2005 |pmid= 16123440 |doi= 10.1167/iovs.05-0007 |doi-access= }}
- {{cite journal |vauthors=Sundin OH, Leppert GS, Silva ED, etal |title=Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=102 |issue= 27 |pages= 9553–8 |year= 2005 |pmid= 15976030 |doi= 10.1073/pnas.0501451102 | pmc=1172243 |bibcode=2005PNAS..102.9553S |doi-access=free }}
- {{cite journal |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 |doi-access= free }}
- {{cite journal |vauthors=Hayward C, Shu X, Cideciyan AV, etal |title=Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration. |journal=Hum. Mol. Genet. |volume=12 |issue= 20 |pages= 2657–67 |year= 2004 |pmid= 12944416 |doi= 10.1093/hmg/ddg289 |doi-access= free }}
{{refend}}
{{protein-stub}}