ADHDgene Database
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Keyword:
Type:
  • Large-scale studies
  • Data Summary
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

Gene Report

Basic Info
Approved Symbol FOXP2
Previous Symbol TNRC10, SPCH1
Symbol Alias CAGH44
Approved Name forkhead box P2
Name Alias trinucleotide repeat containing 10, "forkhead/winged-helix transcription factor", "speech and language disorder 1", "CAG repeat protein 44"
Location 7q31
Position chr7:113726365-114333827, +
External Links HGNC: 13875
Entrez Gene: 93986
Ensembl: ENSG00000128573
UCSC: uc003vgz.2
No. of Studies 1 (significant: 1; non-significant: 0; 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
Ribases, M., 2012 The single-marker and multiple-marker analyses showed an association between FOXP2 and combined ADHD in the German cohort [rs12533005: P=0.0033; odds ratio=1.30 (1.09-1.56); rs12533005/rs1229761: P=4.1e-04; odds ratio=1.38 (1.15-1.66)]. These positive results, however, were not confirmed in the Spanish sample. Significant

Gene related SNPs (count: 123)

Literature-origin SNPs (count: 12)

LD-proxies (count: 111)


Gene related CNVs (count: 0)

Gene related other variant (count: 0)

Gene related regions (count: 0)

Gene related GO terms (count: 31)

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

GO terms by database search (count: 31)


Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with FOXP2 (count: 39)

Genes shared at least 2 KEGG pathways with FOXP2 (count: 0)

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Region: chr7:113726365..114333827 View in gBrowse
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Copyright: Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences Feedback
Last update: Feb 26, 2014