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Symbol Name ID |
Slc5a7
solute carrier family 5 (choline transporter), member 7 MGI:1927126 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ophthalmoparesis |
Ptosis |
| Disease(s) Associated with SLC5A7 | ||
| congenital myasthenic syndrome 20 |
| Mouse Phenotypes | abnormal eye morphology |
retrolental blood |
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| Availability | Mouse Genotype | ||
| Slc5a7tm1a(KOMP)Wtsi/Slc5a7tm1a(KOMP)Wtsi | |||
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 04/30/2024 MGI 6.23 |
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