ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

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)

Literature-origin SNPs (count: 1)

LD-proxies (count: 0)


Gene related CNVs (count: 0)

Gene related other variant (count: 0)

Gene related regions (count: 1)

Gene related GO terms (count: 5)

GO terms by PBA (with statistical significance of FDR<0.05) (count: 0)

GO terms by database search (count: 5)


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)

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Region: chr11:131240373..132206716 View in gBrowse
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