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Symbol Name ID |
Slc9a1
solute carrier family 9 (sodium/hydrogen exchanger), member 1 MGI:102462 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cafe-au-lait spot |
| Disease(s) Associated with SLC9A1 | |
| autosomal recessive spinocerebellar ataxia 19 |
| Mouse Phenotypes | abnormal epidermis stratum corneum morphology |
thin skin |
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| Availability | Mouse Genotype | ||
| Slc9a1tm1Smb/Slc9a1tm1Smb | |||
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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