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

Symbol:	Brinp2tm1.1Pib
Name:	bone morphogenic protein/retinoic acid inducible neural-specific 2; targeted mutation 1.1, Phillip I Bird
MGI ID:	MGI:5604615
Gene:	Brinp2  Location: Chr1:158072839-158183896 bp, - strand  Genetic Position: Chr1, 68.27 cM
Alliance:	Brinp2tm1.1Pib page

Germline Transmission:	Earliest citation of germline transmission: J:244509
Parent Cell Line:	Bruce 4 (ES Cell)
Strain of Origin:	B6.Cg-Thy1a

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: This mutation was generated from the conditional allele by cre recombinase excision of exon 3 and a frt sequence-flanked neomycin resistance cassette in intron 3, leaving a single loxP site. (J:244509)

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 Brinp2 Mutation:	35 strains or lines available

Original:	J:244509 Berkowicz SR, et al., Mice Lacking Brinp2 or Brinp3, or Both, Exhibit Behaviors Consistent with Neurodevelopmental Disorders. Front Behav Neurosci. 2016;10:196
All:	1 reference(s)