ADHDgene Database

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Large-scale studies

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]_7
Symbol in Literature	Patient: 51 (male)
Location	chr11:72900000-73400000 (NCBI Build 35 (hg17))
Type	Duplication
Size	500000 bp
Inheritance	Maternal (affected, also in affected sibling)
Band	11q13.4

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: 9)

Literature-origin genes (count: 0)

Genes from other sources (count: 9)

Approved Symbol	Approved Name	Location	Source
PLEKHB1	pleckstrin homology domain containing, family B (evectins) member 1	11q13.5-q14.1	Mapped by CNV; Mapped by significant region
MRPL48	mitochondrial ribosomal protein L48	11q13.4	Mapped by CNV; Mapped by significant region
UCP3	uncoupling protein 3 (mitochondrial, proton carrier)	11q13.4	Mapped by CNV; Mapped by significant region
RAB6A	RAB6A, member RAS oncogene family	11q13.3	Mapped by CNV; Mapped by significant region
PAAF1	proteasomal ATPase-associated factor 1	11q13.4	Mapped by CNV; Mapped by significant region
CHCHD8	coiled-coil-helix-coiled-coil-helix domain containing 8	11q13.4	Mapped by CNV; Mapped by significant region
FAM168A	family with sequence similarity 168, member A	11q13.4	Mapped by CNV; Mapped by significant region
DNAJB13	DnaJ (Hsp40) homolog, subfamily B, member 13	11q13.3	Mapped by CNV; Mapped by significant region
UCP2	uncoupling protein 2 (mitochondrial, proton carrier)	11q13	Mapped by CNV; Mapped by significant region

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Region: chr11:72900000..73400000 (NCBI Build 35 (hg17)) View in gBrowse
(The coordinate of the CNV has been transformed to NCBI Build 37 (hg19) in gBrowse)