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

Gene Report

Basic Info
Approved Symbol SLC6A19
Approved Name solute carrier family 6 (neutral amino acid transporter), member 19
Name Alias "Hartnup disease"
Location 5p15
Position chr5:1201710-1225232, 1
External Links HGNC: 27960
Entrez Gene: 340024
Ensembl: ENSG00000174358
UCSC: uc003jbw.4
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source Mapped by significant region

Gene related studies (count: 0)

Gene related SNPs (count: 0)

Gene related CNVs (count: 0)

Gene related other variant (count: 0)

Gene related regions (count: 1)

Gene related GO terms (count: 8)

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

GO terms by database search (count: 8)

Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with SLC6A19 (count: 6)

Genes shared at least 2 KEGG pathways with SLC6A19 (count: 0)

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Region: chr5:1201710..1225232 View in gBrowse
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