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| Nomenclature |
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Symbol:
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Slc35c1tm1Cknr
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Name:
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solute carrier family 35, member C1;
targeted mutation 1, Christian Korner
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MGI ID: |
MGI:3709989 |
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Synonyms: |
Slc35c1- |
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Gene:
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Slc35c1
Location:
Chr2:92452764-92460538 bp, - strand
Genetic Position: Chr2,
51.05 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:121151
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Parent Cell Line:
| E14.1 (ES Cell) |
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Strain of Origin:
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129P2/OlaHsd
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutation: | |
Insertion |
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The insertion of a neo into exon 1 resulted in the disruption of the reading frame. (J:121151)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Slc35c1 Mutation:
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0 strains or lines available |
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| References |
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Original: |
J:121151
Hellbusch CC et al.,
"Golgi GDP-fucose transporter-deficient mice mimic congenital disorder of glycosylation IIc/leukocyte adhesion deficiency II."
J Biol Chem 2007 Apr;282(14):10762-72
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All: |
4 reference(s)
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Analysis Tools
