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Symbol
Name
ID
Slc24a1
solute carrier family 24 (sodium/potassium/calcium exchanger), member 1
MGI:2384871
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Congenital stationary night blindness
Blindness
Disease(s) Associated with SLC24A1
congenital stationary night blindness 1D

Mouse Phenotypes
abnormal photoreceptor outer segment morphology
abnormal retinal cone cell outer segment morphology
retinal rod cell degeneration
thin retinal outer nuclear layer
retinal degeneration
abnormal a wave shape
abnormal rod electrophysiology
nyctalopia
Availability Mouse Genotype
Slc24a1tm1Xen/Slc24a1tm1Xen

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
02/04/2020
MGI 6.14
The Jackson Laboratory