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

Symbol:	Cxxc1tm1Skk
Name:	CXXC finger protein 1; targeted mutation 1, David G Skalnik
MGI ID:	MGI:2654854
Synonyms:	CGBP-null
Gene:	Cxxc1  Location: Chr18:74349283-74354564 bp, + strand  Genetic Position: Chr18, 50.7 cM
Alliance:	Cxxc1tm1Skk page

Germline Transmission:	Earliest citation of germline transmission: J:72634
Parent Cell Line:	CCE916 (ES Cell)
Strain of Origin:	129S/SvEv

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: A neomycin selection cassette replaced the entire coding region of the gene, including 5 kb of upstream sequence. (J:72634)

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

In Structures Affected by this Mutation:

3 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 Cxxc1 Mutation:	28 strains or lines available

Original:	J:72634 Carlone DL, et al., Cpg binding protein is crucial for early embryonic development. Mol Cell Biol. 2001 Nov;21(22):7601-6
All:	3 reference(s)