Summary | Mutation origin | Mutation description | Expression | Phenotypes | Disease models | Find Mice (IMSR) | References

Symbol:	Slc35c1tm1Cknr
Name:	solute carrier family 35, member C1; targeted mutation 1, Christian Korner
MGI ID:	MGI:3709989
Synonyms:	Slc35c1-
Gene:	Slc35c1  Location: Chr2:92283109-92290863 bp, - strand  Genetic Position: Chr2, 51.05 cM
Alliance:	Slc35c1tm1Cknr page

Germline Transmission:	Earliest citation of germline transmission: J:121151
Parent Cell Line:	E14.1 (ES Cell)
Strain of Origin:	129P2/OlaHsd

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)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

6 anatomical structure(s)

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:	19 strains or lines available

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)