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

Symbol:	Celsr2tm1Lex
Name:	cadherin, EGF LAG seven-pass G-type receptor 2; targeted mutation 1, Lexicon Genetics
MGI ID:	MGI:5429210
Gene:	Celsr2  Location: Chr3:108298167-108323383 bp, - strand  Genetic Position: Chr3, 47.02 cM
Alliance:	Celsr2tm1Lex page

Germline Transmission:	Earliest citation of germline transmission: J:185566
Parent Cell Line:	Lex-2 (ES Cell)
Strain of Origin:	129S5/SvEvBrd
Project Collection:	Lexicon

Allele Type:    Targeted (Null/knockout) Mutation:    Intragenic deletion     Deletion of coding exons 21-33. (J:185566)

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

In Structures Affected by this Mutation:

1 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 Celsr2 Mutation:	114 strains or lines available

Original:	J:185566 Vogel P, et al., Congenital hydrocephalus in genetically engineered mice. Vet Pathol. 2012 Jan;49(1):166-81
All:	1 reference(s)