NPHP4: Difference between revisions
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Revision as of 19:59, 4 September 2012
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WikiDoc Resources for NPHP4 |
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Articles |
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Media |
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Evidence Based Medicine |
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Clinical Trials |
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Ongoing Trials on NPHP4 at Clinical Trials.gov Clinical Trials on NPHP4 at Google
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Guidelines / Policies / Govt |
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US National Guidelines Clearinghouse on NPHP4
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Books |
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News |
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Commentary |
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Definitions |
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Patient Resources / Community |
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Directions to Hospitals Treating NPHP4 Risk calculators and risk factors for NPHP4
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Healthcare Provider Resources |
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Continuing Medical Education (CME) |
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International |
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Business |
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Experimental / Informatics |
Nephronophthisis 4, also known as NPHP4, is a human gene.[1] This gene encodes a protein which contains a proline-rich region. The encoded protein may function in renal tubular development and function. This protein interacts with nephrocystin. Mutations in this gene are associated with nephronophthisis type 4. Multiple alternative transcript variants have been described but their full-length nature has not been determined.[1]
References
Further reading
- Ishikawa K, Nagase T, Suyama M; et al. (1998). "Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro". DNA Res. 5 (3): 169–76. PMID 9734811.
- Schuermann MJ, Otto E, Becker A; et al. (2002). "Mapping of gene loci for nephronophthisis type 4 and Senior-Løken syndrome, to chromosome 1p36". Am. J. Hum. Genet. 70 (5): 1240–6. PMID 11920287.
- Donaldson JC, Dise RS, Ritchie MD, Hanks SK (2002). "Nephrocystin-conserved domains involved in targeting to epithelial cell-cell junctions, interaction with filamins, and establishing cell polarity". J. Biol. Chem. 277 (32): 29028–35. doi:10.1074/jbc.M111697200. PMID 12006559.
- Otto E, Hoefele J, Ruf R; et al. (2003). "A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution". Am. J. Hum. Genet. 71 (5): 1161–7. PMID 12205563.
- Mollet G, Salomon R, Gribouval O; et al. (2002). "The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin". Nat. Genet. 32 (2): 300–5. doi:10.1038/ng996. PMID 12244321.
- 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. PMID 12477932.
- Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Mollet G, Silbermann F, Delous M; et al. (2005). "Characterization of the nephrocystin/nephrocystin-4 complex and subcellular localization of nephrocystin-4 to primary cilia and centrosomes". Hum. Mol. Genet. 14 (5): 645–56. doi:10.1093/hmg/ddi061. PMID 15661758.
- Hoefele J, Sudbrak R, Reinhardt R; et al. (2006). "Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis". Hum. Mutat. 25 (4): 411. doi:10.1002/humu.9326. PMID 15776426.
- Roepman R, Letteboer SJ, Arts HH; et al. (2006). "Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations". Proc. Natl. Acad. Sci. U.S.A. 102 (51): 18520–5. doi:10.1073/pnas.0505774102. PMID 16339905.
- Szafranski K, Schindler S, Taudien S; et al. "Violating the splicing rules: TG dinucleotides function as alternative 3' splice sites in U2-dependent introns". 8 (8): R154. doi:10.1186/gb-2007-8-8-r154. PMID 17672918.
- Mistry K, Ireland JH, Ng RC; et al. (2007). "Novel mutations in NPHP4 in a consanguineous family with histological findings of focal segmental glomerulosclerosis". Am. J. Kidney Dis. 50 (5): 855–64. doi:10.1053/j.ajkd.2007.08.009. PMID 17954299.