ADHDgene Database

Hot Results

Quick Search

Keyword:
Type:

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

Gene Report

Basic Info

Approved Symbol	NXPH1
Approved Name	neurexophilin 1
Location	7p22
Position	chr7:8473585-8792593, +
External Links	HGNC: 20693 Entrez Gene: 30010 Ensembl: ENSG00000122584 UCSC: uc003srv.2
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin; Mapped by LD-proxy; Mapped by literature SNP

Gene related studies (count: 1)

Reference	Statistical Values/Author Comments	Result of Statistical Analysis
Neale BM, 2010 (b)	No significant or Trend associated SNP was mapped in this gene.	Non-significant

Gene related SNPs (count: 34)

Literature-origin SNPs (count: 2)

rs_ID	Location	Functional Annotation	No. of Studies (significant/non-significant/trend)
rs2107281	Chr7:8636552(Fwd)	intron_variant	1(0/1/0)
rs17151821	Chr7:8628491(Fwd)	intron_variant	1(0/1/0)

LD-proxies (count: 32)

rs_ID	Location	Functional Annotation
rs2214515	Chr7:8611612(Fwd)	intron_variant
rs756465	Chr7:8611075(Fwd)	intron_variant
rs10243253	Chr7:8609625(Fwd)	intron_variant
rs6975588	Chr7:8608191(Fwd)	intron_variant
rs2189463	Chr7:8633637(Fwd)	intron_variant
rs10258143	Chr7:8630769(Fwd)	intron_variant
rs10226547	Chr7:8633143(Fwd)	intron_variant
rs10248829	Chr7:8618880(Fwd)	intron_variant
rs6970999	Chr7:8623087(Fwd)	intron_variant
rs7455385	Chr7:8635606(Fwd)	intron_variant
rs4311585	Chr7:8635638(Fwd)	intron_variant
rs2189465	Chr7:8633836(Fwd)	intron_variant
rs10230697	Chr7:8634212(Fwd)	intron_variant
rs7800185	Chr7:8613465(Fwd)	intron_variant
rs970032	Chr7:8615778(Fwd)	intron_variant
rs10238726	Chr7:8612115(Fwd)	intron_variant
rs7787487	Chr7:8613344(Fwd)	intron_variant
rs6463825	Chr7:8616858(Fwd)	intron_variant
rs2189462	Chr7:8618575(Fwd)	intron_variant
rs6463823	Chr7:8616628(Fwd)	intron_variant
rs6463824	Chr7:8616743(Fwd)	intron_variant
rs10277203	Chr7:8506059(Fwd)	intron_variant
rs7796918	Chr7:8505405(Fwd)	intron_variant
rs10282272	Chr7:8508026(Fwd)	intron_variant
rs17148821	Chr7:8485887(Fwd)	intron_variant
rs2158325	Chr7:8636395(Fwd)	intron_variant
rs10246412	Chr7:8500296(Fwd)	intron_variant
rs2349480	Chr7:8492307(Fwd)	intron_variant
rs4595032	Chr7:8635851(Fwd)	intron_variant
rs4538792	Chr7:8635830(Fwd)	intron_variant
rs4470929	Chr7:8635902(Fwd)	intron_variant
rs4538793	Chr7:8635885(Fwd)	intron_variant

Gene related CNVs (count: 0)

Gene related other variant (count: 0)

Gene related regions (count: 0)

Gene related GO terms (count: 2)

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

GO terms by database search (count: 2)

Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with NXPH1 (count: 0)

Genes shared at least 2 KEGG pathways with NXPH1 (count: 0)

View in gBrowse

Region: chr7:8473585..8792593 View in gBrowse