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

Symbol:	Tctn2tm1.1Reit
Name:	tectonic family member 2; targeted mutation 1.1, Jeremy Reiter
MGI ID:	MGI:5292130
Gene:	Tctn2  Location: Chr5:124736812-124765803 bp, + strand  Genetic Position: Chr5, 63.68 cM, cytoband F
Alliance:	Tctn2tm1.1Reit page

Germline Transmission:	Earliest citation of germline transmission: J:173396
Parent Cell Line:	Other (see notes) (ES Cell)
Strain of Origin:	129P2/OlaHsd

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: A loxP site was inserted upstream of exon 1. A floxed puro cassette was inserted downstream of exon 3. Cre-mediated recombination removed the selection cassette and exons 1 through 3. (J:173396)

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

In Mice Carrying this Mutation:	26 assay results
In Structures Affected by this Mutation:	8 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 Tctn2 Mutation:	22 strains or lines available

Original:	J:173396 Sang L, et al., Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways. Cell. 2011 May 13;145(4):513-28
All:	5 reference(s)