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Symbol
Name
ID
Slc4a11
solute carrier family 4, sodium bicarbonate transporter-like, member 11
MGI:2138987
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Corneal stromal edema
Abnormal corneal endothelium morphology
Abnormal Descemet membrane morphology
Corneal guttata
Descemet Membrane Folds
Reduced number of corneal endothelial cells
Keratitis
Opacification of the corneal stroma
Increased corneal thickness
Corneal degeneration
Corneal dystrophy
Corneal opacity
Nystagmus
Nyctalopia
Visual impairment
Reduced visual acuity
Visual loss
Eye movement-induced pain
Disease(s) Associated with SLC4A11
congenital hereditary endothelial dystrophy of cornea
corneal dystrophy-perceptive deafness syndrome
Fuchs' endothelial dystrophy

Mouse Phenotypes
increased Descemet membrane thickness
increased cornea thickness
abnormal corneal endothelium morphology
abnormal corneal epithelium morphology
increased corneal epithelium thickness
abnormal corneal stroma morphology
increased corneal stroma thickness
corneal deposits
corneal opacity
Availability Mouse Genotype
Slc4a11Gt(OST443317)Lex/Slc4a11Gt(OST443317)Lex
Slc4a11tm1.1Jrcy/Slc4a11tm1.1Jrcy
Slc4a11tm1Boet/Slc4a11tm1Boet

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory