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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc24a1
solute carrier family 24 (sodium/potassium/calcium exchanger), member 1
MGI:2384871
8 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc24a1tm1Xen/Slc24a1tm1Xen
involves: C57BL/6
abnormal a-wave shape J:226323
abnormal photoreceptor outer segment morphology J:226323
abnormal rod electrophysiology J:226323
increased susceptibility to age-related retinal degeneration J:226323
nyctalopia J:226323
retina rod cell degeneration J:226323
short retina cone cell outer segment J:226323
thin retina outer nuclear layer J:226323

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
04/09/2024
MGI 6.23
The Jackson Laboratory