ADHDgene Database

Gene Report

Basic Info

Approved Symbol	CNTN5
Symbol Alias	NB-2, hNB-2
Approved Name	contactin 5
Location	11q21-q22.2
Position	chr11:98891683-100229616, +
External Links	HGNC: 2175 Entrez Gene: 53942 Ensembl: ENSG00000149972 UCSC: uc001pga.2
No. of Studies	1 (significant: 0; non-significant: 0; trend: 1)
Source	Literature-origin; Mapped by CNV; Mapped by significant region

Gene related studies (count: 1)

Reference	Statistical Values/Author Comments	Result of Statistical Analysis
Lionel, A. C., 2011	De novo and/or rare inherited CNVs associated with this gene were detected for not only ADHD, but also other neurodevelopmental conditions including ASD.	Trend

Gene related SNPs (count: 0)

Gene related CNVs (count: 1)

ID	Location	Size	Band	Type	Inheritance
CNV_Lionel[2011]_21	chr11:0-0 (NCBI36 / hg18)	49	11q22.1	Loss	P

Gene related other variant (count: 0)

Gene related regions (count: 2)

Region Name	Position	No. of Studies (significant/non-significant/trend)
11q	chr11:53700000-135006516	2 (1/1/0)
11q22	chr11:97200000-110400000	1 (1/0/0)

Gene related GO terms (count: 5)

ID	Name	Type	No. of Genes in ADHDgene
GO:0005886	plasma membrane	Cellular Component	772
GO:0005737	cytoplasm	Cellular Component	690
GO:0007605	sensory perception of sound	Biological Process	31
GO:0007155	cell adhesion	Biological Process	86
GO:0031225	anchored to membrane	Cellular Component	29

Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with CNTN5 (count: 0)

Genes shared at least 2 KEGG pathways with CNTN5 (count: 0)

View in gBrowse

Region: chr11:98891683..100229616 View in gBrowse