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 chr20:3227417-3239190, -1
External Links HGNC: 16438
Entrez Gene: 83959
Ensembl: ENSG00000088836
UCSC: uc010zqe.2
No. of Studies 1 (Positive: 0; Negative: 1; trend: 0)
Overlap with SZ? NO
Overlap with MDD? NO
Gene related studies (count: 1)
Reference Tested Markers Statistical Values/Author Comments Result Category Comment on Study
Xu, W., 2014 SNP: rs2014425 The SNP within or near this gene did not achieve genome-wide significance. Negative Comment on Study
Gene functional annotation
Gene related GO terms (count: 18)

GO terms by PBA (count: 2)

GO terms by database search (count: 16)

Gene related KEGG pathways (count: 0)

Gene related BioCarta pathways (count: 0)

Gene related interactors from protein-protein interactions data in HPRD (count: 0)

Related other genetic factors
Gene related SNPs (count: 1)

Literature-origin SNPs (count: 1)

LD-proxies (count: 0)

Gene related CNVs (count: 0)

Gene related other variants (count: 0)

Gene related regions (count: 3)

Overlap with schizophrenia (SZ) and major depressive disorder (MDD)
Gene relationship with SZ

Gene relationship with MDD

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Region: chr20:3227417..3239190 View in gBrowse
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