ADHDgene Database

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Type:

Large-scale studies

Genome-wide Association Studies of ADHD
Genome-wide Linkage Studies of ADHD
Genome-wide CNV Analyses of ADHD
Meta-analysis Studies of ADHD

Data Summary

Published Variant
- SNP: 1391
- CNV: 398
- Others: 173
Published Gene: 359
Published Region: 128
Pathway by PBA: 8
Study: 361

Detail ...

CNV Report

Basic Info

Name	CNV_Lesch[2011]_9
Symbol in Literature	Patient: 1191 (male)
Location	chr2:660000-940000 (NCBI Build 35 (hg17))
Type	Duplication
Size	280000 bp
Inheritance	Maternal (healthy)
Band	2p25.3

CNV related studies (count: 1)

Reference	Author Comments
Lesch KP, 2011	The aberrations are likely ADHD-associated, based on the fact that they are not documented in the reference data sets. The aberrations are likely ADHD-associated, based on the fact that they are not documented in the reference data sets.

CNV related genes (count: 2)

Literature-origin genes (count: 0)

Genes from other sources (count: 2)

Approved Symbol	Approved Name	Location	Source
TMEM18	transmembrane protein 18	2p25.3	Mapped by CNV
SNTG2	syntrophin, gamma 2	2p25	Mapped by CNV

View in gBrowse

Region: chr2:660000..940000 (NCBI Build 35 (hg17)) View in gBrowse
(The coordinate of the CNV has been transformed to NCBI Build 37 (hg19) in gBrowse)