ADHDgene Database

Gene Report

Basic Info

Approved Symbol	NTM
Symbol Alias	HNT, NTRI, IGLON2
Approved Name	neurotrimin
Name Alias	"neurotrimin", "IgLON family member 2"
Location	11q25
Position	chr11:131240373-132206716, 1
External Links	HGNC: 17941 Entrez Gene: 50863 Ensembl: ENSG00000182667 UCSC: uc001qgq.3
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin; Mapped by Literature SNP; Mapped by significant region

Gene related studies (count: 1)

Reference	Statistical Values/Author Comments	Result of Statistical Analysis
Yang L, 2013	Gene with smallest SNP P-value=0.0000474, no significant or Trend associated SNP was mapped in this gene.	Non-significant

Gene related SNPs (count: 1)

rs_ID	Location	Functional Annotation	No. of Studies (significant/non-significant/trend)
rs1940028	chr11:131842743(Fwd)	intron_variant; nc_transcript_variant	1(0/1/0)

Gene related CNVs (count: 0)

Gene related other variant (count: 0)

Gene related regions (count: 1)

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

Gene related GO terms (count: 5)

ID	Name	Type	Evidence[PMID]	No. of Genes in ADHDgene
GO:0005886	plasma membrane	cellular component	IEA	839
GO:0008038	neuron recognition	biological process	TAS[7891157]	4
GO:0031225	anchored to membrane	cellular component	IEA	33
GO:0007155	cell adhesion	biological process	IEA	99
GO:0005515	protein binding	molecular function	IPI	1015

Gene related KEGG pathways (count: 0)

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

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

View in gBrowse

Region: chr11:131240373..132206716 View in gBrowse