Slc35c1^tm1Cknr
Targeted Allele Detail

Summary

• Symbol: Slc35c1^tm1Cknr
• 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: Slc35c1^tm1Cknr page

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)

Disease models

Expression

In Structures Affected by this Mutation:

6 anatomical structure(s)

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: 19 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: 5 reference(s)