CDH9
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Protein-coding gene in humans
| CDH9 | |||||||||||||||||||||||||||||||||||||||||||||||
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| Aliases | CDH9 , cadherin 9 | ||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 609974; MGI: 107433; HomoloGene: 9450; GeneCards: CDH9; OMA:CDH9 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||
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Cadherin 9 is a protein that in humans is encoded by the CDH9 gene.[5] [6]
Clinical significance
[edit ]An association with autism has been suggested.[7]
See also
[edit ]References
[edit ]- ^ a b c GRCh38: Ensembl release 89: ENSG00000113100 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025370 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: cadherin 9".
- ^ Suzuki S, Sano K, Tanihara H (April 1991). "Diversity of the cadherin family: evidence for eight new cadherins in nervous tissue". Cell Regulation. 2 (4): 261–70. doi:10.1091/mbc.2.4.261. PMC 361775 . PMID 2059658.
- ^ Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, et al. (May 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.
External links
[edit ]- Human CDH9 genome location and CDH9 gene details page in the UCSC Genome Browser.
Further reading
[edit ]- Nollet F, Kools P, van Roy F (June 2000). "Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members". Journal of Molecular Biology. 299 (3): 551–72. doi:10.1006/jmbi.2000.3777. PMID 10835267.
- Shimoyama Y, Tsujimoto G, Kitajima M, Natori M (July 2000). "Identification of three human type-II classic cadherins and frequent heterophilic interactions between different subclasses of type-II classic cadherins". The Biochemical Journal. 349 (Pt 1): 159–67. doi:10.1042/0264-6021:3490159. PMC 1221133 . PMID 10861224.
- Wang K, Zhang H, Bloss CS, Duvvuri V, Kaye W, Schork NJ, Berrettini W, Hakonarson H (September 2011). "A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa". Molecular Psychiatry. 16 (9): 949–59. doi:10.1038/mp.2010.107. PMC 3859494 . PMID 21079607.
- Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T, Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K, Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T, Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T, Sugano S (January 2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Research. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129 . PMID 16344560.
- Ali J, Liao F, Martens E, Muller WA (June 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.
- Thedieck C, Kalbacher H, Kuczyk M, Müller GA, Müller CA, Klein G (2007). Zoccali C (ed.). "Cadherin-9 is a novel cell surface marker for the heterogeneous pool of renal fibroblasts". PLOS ONE. 2 (7): e657. Bibcode:2007PLoSO...2..657T. doi:10.1371/journal.pone.0000657 . PMC 1924602 . PMID 17668045. Open access icon
- Hülsken J, Birchmeier W, Behrens J (December 1994). "E-cadherin and APC compete for the interaction with beta-catenin and the cytoskeleton". The Journal of Cell Biology. 127 (6 Pt 2): 2061–9. doi:10.1083/jcb.127.6.2061. PMC 2120290 . PMID 7806582.
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