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Symbol
Name
ID

Slc35c1
solute carrier family 35, member C1
MGI:2443301

Phenotype annotations related to hematopoietic system

Darker colors indicate more annotations

Human Phenotypes	Neutrophilia	Reduction of neutrophil motility
Disease(s) Associated with SLC35C1	Neutrophilia	Reduction of neutrophil motility
congenital disorder of glycosylation type IIc

Mouse Phenotypes		impaired leukocyte tethering or rolling	abnormal leukocyte adhesion	increased eosinophil cell number	increased neutrophil cell number	increased lymphocyte cell number	increased monocyte cell number	increased leukocyte cell number
Availability	Mouse Genotype
	Slc35c1^tm1Cknr/Slc35c1^tm1Cknr

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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