| Human Disease |
Congenital Disorder of Glycosylation, Type IIC; CDG2C OMIM ID: 266265 |
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| Synonyms | Cdg IIC; CDGIIC; Leukocyte Adhesion Deficiency, Type II; LAD2; Rambam-Hasharon Syndrome; RHS | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc35c1tm1Cknr/Slc35c1tm1Cknr |
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 | J:121151 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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