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

Gene Report

Basic Info
Approved Symbol DYX1C1
Symbol Alias EKN1, FLJ37882
Approved Name dyslexia susceptibility 1 candidate 1
Location 15q21.1
Position chr15:55702723-55800432, -
External Links HGNC: 21493
Entrez Gene: 161582
Ensembl: ENSG00000256061
UCSC: uc002adc.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
Wigg KG, 2008 haplotypes of the six markers P-value=0.078, X2=6.809, df=1, no significant association Non-significant

Gene related SNPs (count: 28)

Literature-origin SNPs (count: 6)

LD-proxies (count: 22)

Gene related CNVs (count: 0)

Gene related other variant (count: 1)

Gene related regions (count: 0)

Gene related GO terms (count: 7)

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

GO terms by database search (count: 7)

Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with DYX1C1 (count: 0)

Genes shared at least 2 KEGG pathways with DYX1C1 (count: 0)

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Region: chr15:55702723..55800432 View in gBrowse
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