Sandbox Reserved 1234
From Proteopedia
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RPGR consist of 28 beta sheets and 4 alpha helices. It also contains a glutamate rich region [1]. | RPGR consist of 28 beta sheets and 4 alpha helices. It also contains a glutamate rich region [1]. | ||
== Function == | == Function == | ||
- | RPGR essentially provides normal vision. This protein is known to localize the outer segments of rod photoreceptors. It plays a role in ciliogenesis, photoreceptor integrity, and spermatogenesis. The cilia are fingerlike projections from the cell that aid in its movement [5]. It has the ability to regulate the cilia by regulating the actin stress filaments [ | + | RPGR essentially provides normal vision. This protein is known to localize the outer segments of rod photoreceptors. It plays a role in ciliogenesis, photoreceptor integrity, and spermatogenesis. The cilia are fingerlike projections from the cell that aid in its movement [5]. It has the ability to regulate the cilia by regulating the actin stress filaments [5]. It is localized in the Golgi apparatus. |
== Related Disease == | == Related Disease == | ||
Ciliopathies are caused by defects to the cilia. Ciliopathies include kidney disease, nephronophtisis, Bardet–Biedl syndrome (BBS) and retinal degeneration syndromes [3]. Retinitis pigmentosa is an eye disease that cause the photoreceptors cells to degenerate [3]. More than 300 mutations to the RPGR may cause retinitis pigmentosa and make up 70% of the occurrences [3]. These mutations usually cause the protein to be shortened and malfunction. Once there is degeneration, night blindness may occur and eventually complete loss of vision. This disease may lead to other ciliopathy phenotypes such as respiratory infection, hearing defects, and abnormal sperm. Retinitis pigmentosa GTPase regulator is also connected to a more severe disease, X-linked retinitis pigmentosa. | Ciliopathies are caused by defects to the cilia. Ciliopathies include kidney disease, nephronophtisis, Bardet–Biedl syndrome (BBS) and retinal degeneration syndromes [3]. Retinitis pigmentosa is an eye disease that cause the photoreceptors cells to degenerate [3]. More than 300 mutations to the RPGR may cause retinitis pigmentosa and make up 70% of the occurrences [3]. These mutations usually cause the protein to be shortened and malfunction. Once there is degeneration, night blindness may occur and eventually complete loss of vision. This disease may lead to other ciliopathy phenotypes such as respiratory infection, hearing defects, and abnormal sperm. Retinitis pigmentosa GTPase regulator is also connected to a more severe disease, X-linked retinitis pigmentosa. |
Current revision
RPGR- Retinitis Pigmentosa GTPase Regulator
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References
[1] http://www.rcsb.org/pdb/explore/explore.do?structureId=4JHP [2] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3642377/ [3] https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/ddw281 [4] http://www.genecards.org/cgi-bin/carddisp.pl?gene=RPGR&keywords=4jhp [5] https://ghr.nlm.nih.gov/gene/RPGR