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Symbol Name ID |
Slc35c1
solute carrier family 35, member C1 MGI:2443301 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of metabolism/homeostasis |
| Disease(s) Associated with SLC35C1 | |
| congenital disorder of glycosylation type IIc |
| Mouse Phenotypes | abnormal metabolism |
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| Availability | Mouse Genotype | |
| Slc35c1tm1Cknr/Slc35c1tm1Cknr | ||
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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