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

Symbol:	Bbip1tm1.1Gne
Name:	BBSome interacting protein 1; targeted mutation 1.1, Genentech
MGI ID:	MGI:5563473
Gene:	Bbip1  Location: Chr19:53918292-53933058 bp, - strand  Genetic Position: Chr19, 48.8 cM
Alliance:	Bbip1tm1.1Gne page

Germline Transmission:	Earliest citation of germline transmission: J:204140
Parent Cell Line:	C2 (Nagy) (ES Cell)
Strain of Origin:	C57BL/6NTac

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: A loxP site was inserted upstream of exon 2 and an FRT flanked pgk-em7-neo cassette and loxP site were inserted downstream of exon 2. Cre mediated recombination removed exon 2 and the pgk-em7-neo cassette. (J:204140)

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 Bbip1 Mutation:	19 strains or lines available

Original:	J:204140 Loktev AV, et al., Neuropeptide Y Family Receptors Traffic via the Bardet-Biedl Syndrome Pathway to Signal in Neuronal Primary Cilia. Cell Rep. 2013 Dec 12;5(5):1316-29
All:	2 reference(s)