protocadherin-11 X-linked isoform X2 [Homo sapiens]

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Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia. [Am J Med Genet B Neuropsychiat...]
Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia.
Veerappa AM, Saldanha M, Padakannaya P, Ramachandra NB. Am J Med Genet B Neuropsychiatr Genet. 2013 Dec; 162B(8):889-97. Epub 2013 Sep 20.
Lack of association between PCDH11X genetic variation and late-onset Alzheimer's disease in a Han Chinese population. [Brain Res. 2010]
Lack of association between PCDH11X genetic variation and late-onset Alzheimer's disease in a Han Chinese population.
Wu ZC, Yu JT, Wang ND, Yu NN, Zhang Q, Chen W, Zhang W, Zhu QX, Tan L. Brain Res. 2010 Oct 21; 1357:152-6. Epub 2010 Aug 11.
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients. [J Alzheimers Dis. 2010]
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients.
Lescai F, Pirazzini C, D'Agostino G, Santoro A, Ghidoni R, Benussi L, Galimberti D, Federica E, Marchegiani F, Cardelli M, et al. J Alzheimers Dis. 2010; 21(2):385-8.

RefSeq genomic sequence
See the genomic reference sequence for the PCDH11X gene (NG_016251.1).
RefSeq mRNA
See reference mRNA sequence for the PCDH11X gene (XM_054326839.1).
RefSeq protein isoforms
See 23 reference sequence protein isoforms for the PCDH11X gene.

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Protein