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Symbol
Name
ID
Slc35c1
solute carrier family 35, member C1
MGI:2443301
Phenotype annotations related to growth/size/body
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
Availability Mouse Genotype
Slc35c1tm1Cknr/Slc35c1tm1Cknr

Contributing Projects:
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
04/09/2024
MGI 6.23
The Jackson Laboratory