DYX1C1

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Dyslexia susceptibility 1 candidate 1
Identifiers
Symbol(s) DYX1C1; DYX1; RD; DYXC1; EKN1; FLJ37882; MGC70618
External IDs OMIM: 608706 MGI: 1914935 HomoloGene: 12173
Orthologs
Human Mouse
Entrez 161582 67685
Ensembl n/a ENSMUSG00000032210
Uniprot n/a Q5VJS4
Refseq NM_001033559 (mRNA)
NP_001028731 (protein)		 NM_026314 (mRNA)
NP_080590 (protein)
Location n/a Chr 9: 72.76 - 72.77 Mb
Pubmed search [1] [2]

Dyslexia susceptibility 1 candidate 1, also known as DYX1C1, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: DYX1C1 dyslexia susceptibility 1 candidate 1.

[edit] Further reading

  • Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery.". Genome Res. 6 (9): 791-806. PMID 8889548. 
  • 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. 
  • Taipale M, Kaminen N, Nopola-Hemmi J, et al. (2003). "A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.". Proc. Natl. Acad. Sci. U.S.A. 100 (20): 11553-8. doi:10.1073/pnas.1833911100. PMID 12954984. 
  • 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. 
  • Wigg KG, Couto JM, Feng Y, et al. (2005). "Support for EKN1 as the susceptibility locus for dyslexia on 15q21.". Mol. Psychiatry 9 (12): 1111-21. doi:10.1038/sj.mp.4001543. PMID 15249932. 
  • Ylisaukko-Oja T, Peyrard-Janvid M, Lindgren CM, et al. (2005). "Family-based association study of DYX1C1 variants in autism.". Eur. J. Hum. Genet. 13 (1): 127-30. doi:10.1038/sj.ejhg.5201272. PMID 15470369. 
  • Cope NA, Hill G, van den Bree M, et al. (2005). "No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia.". Mol. Psychiatry 10 (3): 237-8. doi:10.1038/sj.mp.4001596. PMID 15477871. 
  • 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. PMID 15489334. 
  • Scerri TS, Fisher SE, Francks C, et al. (2005). "Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.". J. Med. Genet. 41 (11): 853-7. doi:10.1136/jmg.2004.018341. PMID 15520411. 
  • Marino C, Citterio A, Giorda R, et al. (2007). "Association of short-term memory with a variant within DYX1C1 in developmental dyslexia.". Genes Brain Behav. 6 (7): 640-6. doi:10.1111/j.1601-183X.2006.00291.x. PMID 17309662. 
  • Brkanac Z, Chapman NH, Matsushita MM, et al. (2007). "Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.". Am. J. Med. Genet. B Neuropsychiatr. Genet. 144 (4): 556-60. doi:10.1002/ajmg.b.30471. PMID 17450541. 
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