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_Williams[2010]_25
Symbol in Literature	Sample ID: 25 (case)
Location	chr20:12795614-14242196 (NCBI Build 36.1 (hg18))
Type	Gain
Size	1394171 bp
Band	20p12.1

CNV related studies (count: 1)

Reference	Author Comments
Williams NM, 2010	Rare CNV larger than 500kb identified in children with ADHD. Rare CNV larger than 500kb identified in children with ADHD.

CNV related genes (count: 12)

Literature-origin genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
MACROD2	MACRO domain containing 2	20p12.1	1(0/0/1)

Genes from other sources (count: 11)

Approved Symbol	Approved Name	Location	Source
TASP1	taspase, threonine aspartase, 1	20p12	Mapped by CNV
GAPDHP2	glyceraldehyde-3-phosphate dehydrogenase pseudogene 2	20p12.1	Mapped by CNV
ISM1	isthmin 1 homolog (zebrafish)	20p12.1	Mapped by CNV
ESF1	ESF1, nucleolar pre-rRNA processing protein, homolog (S. cerevisiae)	20p12.1	Mapped by CNV
SPTLC3	serine palmitoyltransferase, long chain base subunit 3	20p12.1	Mapped by CNV
SCYE1P	small inducible cytokine subfamily E, member 1 (endothelial monocyte-activating) pseudogene	20	Mapped by CNV
RPS3P1	ribosomal protein S3 pseudogene 1	20p12	Mapped by CNV
SEL1L2	sel-1 suppressor of lin-12-like 2 (C. elegans)	20p12.1	Mapped by CNV
TRNAE43P	transfer RNA glutamic acid 43 (anticodon CUC) pseudogene	20p12.1	Mapped by CNV
MRPS36P6	mitochondrial ribosomal protein S36 pseudogene 6	20p12.1	Mapped by CNV
C20orf7	chromosome 20 open reading frame 7	20p12.1	Mapped by CNV

View in gBrowse

Region: chr20:12795614..14242196 (NCBI Build 36.1 (hg18)) View in gBrowse
(The coordinate of the CNV has been transformed to NCBI Build 37 (hg19) in gBrowse)