Symbol Name ID |
Slc35c1
solute carrier family 35, member C1 MGI:2443301 |
Darker colors indicate more annotations |
Human Phenotypes | Short stature |
Disease(s) Associated with SLC35C1 | |
congenital disorder of glycosylation type IIc |
Mouse Phenotypes | decreased body weight |
postnatal growth retardation |
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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 05/28/2024 MGI 6.13 |
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