Symbol Name ID |
Slc35c1
solute carrier family 35, member C1 MGI:2443301 |
Darker colors indicate more annotations |
Human Phenotypes | Neutrophilia |
Reduction of neutrophil motility |
Periodontitis |
Recurrent otitis media |
Pneumonia |
Bronchiolitis |
Cellulitis |
Disease(s) Associated with SLC35C1 | |||||||
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 |
abnormal lymph node primary follicle morphology |
lymph node hypoplasia |
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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 04/23/2024 MGI 6.23 |
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