3q26.1del_human-BCHE

General

Gene Locus : human-BCHE

Mode of mutation : Natural mutant

Disease :

Summary : Expression No expression Lesch_2011_Mol.Psychiatry_16_491

AAA Change :

Allelic Variant :

Risk Factor :

Inhibitor :

Structure :

Disease by interaction :

Interact Gene Locus :

Xenobiotic sensitivity : Defect in Suxamethonium hydrolysis

Modification : Expression

Torpedo_number : No torpedo number

Kinetic Parameter : No kinetic parameter

News : No news

Comment : 3q26.1del Genome-wide copy number variation analysis in attention-deficit\/hyperactivity disorder. One is a de novo chromosome 3q26.1 deletion. BChE not likely to be involved

References (1)

Title : Genome-wide copy number variation analysis in attention-deficit\/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree - Lesch_2011_Mol.Psychiatry_16_491
Author(s) : Lesch KP , Selch S , Renner TJ , Jacob C , Nguyen TT , Hahn T , Romanos M , Walitza S , Shoichet S , Dempfle A , Heine M , Boreatti-Hummer A , Romanos J , Gross-Lesch S , Zerlaut H , Wultsch T , Heinzel S , Fassnacht M , Fallgatter A , Allolio B , Schafer H , Warnke A , Reif A , Ropers HH , Ullmann R
Ref : Mol Psychiatry , 16 :491 , 2011
Abstract : Lesch_2011_Mol.Psychiatry_16_491
ESTHER : Lesch_2011_Mol.Psychiatry_16_491
PubMedSearch : Lesch_2011_Mol.Psychiatry_16_491
PubMedID: 20308990