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Slc35c1tm1Cknr
Targeted Allele Detail
Nomenclature
Symbol: Slc35c1tm1Cknr
Name: solute carrier family 35, member C1; targeted mutation 1, Christian Korner
MGI ID: MGI:3709989
Synonyms: Slc35c1-
Gene: Slc35c1  Location: Chr2:92452764-92460538 bp, - strand  Genetic Position: Chr2, 51.05 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:121151
Parent Cell Line:  E14.1 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Insertion
    The insertion of a neo into exon 1 resulted in the disruption of the reading frame. (J:121151)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Slc35c1 Mutation:  13 strains or lines available
References
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
All:  4 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/15/2018
MGI 6.12
The Jackson Laboratory