IMPG1
Interphotoreceptor matrix proteoglycan 1 is a protein that in humans is encoded by the IMPG1 gene.[1]
References
Further reading
- Felbor U, Gehrig A, Sauer CG, et al. (1998). “Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies”. Cytogenet. Cell Genet. 81 (1): 12–7. doi:10.1159/000015001. PMID 9691169.
- Gehrig A, Felbor U, Kelsell RE, et al. (1998). “Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)”. J. Med. Genet. 35 (8): 641–5. doi:10.1136/jmg.35.8.641. PMC 1051388. PMID 9719369.
- Acharya S, Rayborn ME, Hollyfield JG (1998). “Characterization of SPACR, a sialoprotein associated with cones and rods present in the interphotoreceptor matrix of the human retina: immunological and lectin binding analysis”. Glycobiology. 8 (10): 997–1006. doi:10.1093/glycob/8.10.997. PMID 9719680.
- Acharya S, Rodriguez IR, Moreira EF, et al. (1998). “SPACR, a novel interphotoreceptor matrix glycoprotein in human retina that interacts with hyaluronan”. J. Biol. Chem. 273 (47): 31599–606. doi:10.1074/jbc.273.47.31599. PMID 9813076.
- Kuehn MH, Hageman GS (2000). “Expression and characterization of the IPM 150 gene (IMPG1) product, a novel human photoreceptor cell-associated chondroitin-sulfate proteoglycan”. Matrix Biol. 18 (5): 509–18. doi:10.1016/S0945-053X(99)00043-8. PMID 10601738.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Mungall AJ, Palmer SA, Sims SK, et al. (2003). “The DNA sequence and analysis of human chromosome 6”. Nature. 425 (6960): 805–11. doi:10.1038/nature02055. PMID 14574404.
- van Lith-Verhoeven JJ, Hoyng CB, van den Helm B, et al. (2004). “The benign concentric annular macular dystrophy locus maps to 6p12.3-q16”. Invest. Ophthalmol. Vis. Sci. 45 (1): 30–5. doi:10.1167/iovs.03-0392. PMID 14691150.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Abd El-Aziz MM, El-Ashry MF, Barragan I, et al. (2006). “Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus”. Curr. Eye Res. 30 (12): 1081–7. doi:10.1080/02713680500351039. PMID 16354621.
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