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Symbol Name ID |
Slc24a1
solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 MGI:2384871 |
| Darker colors indicate more annotations |
| Human Phenotypes | Attenuation of retinal blood vessels |
Macular atrophy |
Pigmentary retinopathy |
Congenital stationary night blindness |
| Disease(s) Associated with SLC24A1 | ||||
| congenital stationary night blindness 1D |
| Mouse Phenotypes | abnormal photoreceptor outer segment morphology |
short retina cone cell outer segment |
retina rod cell degeneration |
thin retina outer nuclear layer |
increased susceptibility to age-related retinal degeneration |
abnormal a-wave shape |
abnormal rod electrophysiology |
nyctalopia |
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| Availability | Mouse Genotype | ||||||||
| Slc24a1tm1Xen/Slc24a1tm1Xen | |||||||||
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 04/16/2024 MGI 6.23 |
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