Protein-coding gene in humans
Cadherin 10 is a protein that in humans is encoded by the CDH10 gene .[ 5] [ 6]
Clinical significance An association with autism has been suggested.[ 7]
See also
References
External links
Further reading
Stelzl U, Worm U, Lalowski M, et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell . 122 (6): 957–68. doi :10.1016/j.cell.2005.08.029 . hdl :11858/00-001M-0000-0010-8592-0 PMID 16169070 . S2CID 8235923 . Rose JE, Behm FM, Drgon T, et al. (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score" . Mol. Med . 16 (7–8): 247–53. doi :10.2119/molmed.2009.00159 . PMC 2896464 PMID 20379614 . Shimoyama Y, Tsujimoto G, Kitajima M, Natori M (2000). "Identification of three human type-II classic cadherins and frequent heterophilic interactions between different subclasses of type-II classic cadherins" . Biochem. J . 349 (Pt 1): 159–67. doi :10.1042/0264-6021:3490159 . PMC 1221133 PMID 10861224 . Wang K, Zhang H, Ma D, et al. (2009). "Common genetic variants on 5p14.1 associate with autism spectrum disorders" . Nature . 459 (7246): 528–33. Bibcode :2009Natur.459..528W . doi :10.1038/nature07999 . PMC 2943511 PMID 19404256 . Potkin SG, Guffanti G, Lakatos A, et al. (2009). "Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease" . PLOS ONE . 4 (8): e6501. Bibcode :2009PLoSO...4.6501P . doi :10.1371/journal.pone.0006501 PMC 2719581 PMID 19668339 . Gil OD, Needleman L, Huntley GW (2002). "Developmental patterns of cadherin expression and localization in relation to compartmentalized thalamocortical terminations in rat barrel cortex". J. Comp. Neurol . 453 (4): 372–88. doi :10.1002/cne.10424 . PMID 12389209 . S2CID 25610258 . Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes" . Genome Res . 16 (1): 55–65. doi :10.1101/gr.4039406 . PMC 1356129 PMID 16344560 . Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "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. Bibcode :2002PNAS...9916899M . doi :10.1073/pnas.242603899 PMC 139241 PMID 12477932 . Kools P, Vanhalst K, Van den Eynde E, van Roy F (1999). "The human cadherin-10 gene: complete coding sequence, predominant expression in the brain, and mapping on chromosome 5p13-14" . FEBS Lett . 452 (3): 328–34. doi :10.1016/S0014-5793(99)00672-9 PMID 10386616 . S2CID 44714251 . Hillier LD, Lennon G, Becker M, et al. (1996). "Generation and analysis of 280,000 human expressed sequence tags" . Genome Res . 6 (9): 807–28. doi :10.1101/gr.6.9.807 PMID 8889549 . Ali J, Liao F, Martens E, Muller WA (1997). "Vascular endothelial cadherin (VE-cadherin): cloning and role in endothelial cell-cell adhesion". Microcirculation . 4 (2): 267–77. doi :10.3109/10739689709146790 . PMID 9219219 . S2CID 21501093 . Ma D, Salyakina D, Jaworski JM, et al. (2009). "A genome-wide association study of autism reveals a common novel risk locus at 5p14.1" . Ann. Hum. Genet . 73 (Pt 3): 263–73. doi :10.1111/j.1469-1809.2009.00523.x . PMC 2918410 PMID 19456320 . Hülsken J, Birchmeier W, Behrens J (1994). "E-cadherin and APC compete for the interaction with beta-catenin and the cytoskeleton" . J. Cell Biol . 127 (6 Pt 2): 2061–9. doi :10.1083/jcb.127.6.2061 . PMC 2120290 PMID 7806582 .
