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

Gene Report

Basic Info
Approved Symbol SLC4A11
Previous Symbol CHED2, CDPD1
Symbol Alias dJ794I6.2, BTR1, NaBC1, FECD4
Approved Name solute carrier family 4, sodium borate transporter, member 11
Previous Name "corneal endothelial dystrophy 2 (autosomal recessive)", "solute carrier family 4, sodium bicarbonate transporter-like, member 11", "corneal dystrophy and perceptive deafness 1"
Location 20p13
Position chr20:3208063-3219836, -1
External Links HGNC: 16438
Entrez Gene: 83959
Ensembl: ENSG00000088836
UCSC: uc010zqe.2
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source Mapped by CNV

Gene related studies (count: 0)

Gene related SNPs (count: 0)

Gene related CNVs (count: 1)

Gene related other variant (count: 0)

Gene related regions (count: 0)

Gene related GO terms (count: 18)

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

GO terms by database search (count: 18)

Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with SLC4A11 (count: 0)

Genes shared at least 2 KEGG pathways with SLC4A11 (count: 0)

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Region: chr20:3208063..3219836 View in gBrowse
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