Variant: rs1554008611 

    present in Gene: CTNND2
    present in Chromosome: 5
    Position on Chromosome: 11236825
    Alleles of this Variant: T/C

rs1554008611 in CTNND2 gene and Movement Disorders PMID 25839933 2015 CTNND2 deletion and intellectual disability.

PMID 25807484 2015 Loss of δ-catenin function in severe autism.

PMID 26601658 2016 Multigenerational autosomal dominant inheritance of 5p chromosomal deletions.

PMID 25473103 2015 CTNND2-a candidate gene for reading problems and mild intellectual disability.

PMID 29127138 2017 δ-Catenin (CTNND2) missense mutation in familial cortical myoclonic tremor and epilepsy.

PMID 25106414 2014 The clinical significance of small copy number variants in neurodevelopmental disorders.

PMID 15733271 2005 A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.

PMID 12835311 2003 Dual regulation of neuronal morphogenesis by a delta-catenin-cortactin complex and Rho.