Symbol Name ID |
Slc35c1
solute carrier family 35, member C1 MGI:2443301 |
Darker colors indicate more annotations |
Human Phenotypes | Widow's peak |
Abnormality of the integument |
Disease(s) Associated with SLC35C1 | ||
congenital disorder of glycosylation type IIc |
Mouse Phenotypes | ruffled hair |
|
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) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|