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

Symbol:	Brinp2em1(IMPC)Wtsi
Name:	bone morphogenic protein/retinoic acid inducible neural-specific 2; endonuclease-mediated mutation 1, Wellcome Trust Sanger Institute
MGI ID:	MGI:6286377
Gene:	Brinp2  Location: Chr1:158072839-158183896 bp, - strand  Genetic Position: Chr1, 68.27 cM
Alliance:	Brinp2em1(IMPC)Wtsi page
IMPC:	Brinp2 gene page

Strain of Origin:	C57BL/6N
Project Collection:	IMPC

Allele Type:    Endonuclease-mediated (Null/knockout) Mutation:    Intragenic deletion   Mutation details: This allele from IMPC was generated at Welcome Sanger Institute by injecting CAS9 RNA and 4 guide sequences CCACAGTGCCCTTCCCACGGGGT, CCTCCCCTCTGGATGAGAATAGA, AGTAGAAGAGGCTCCTCCTCTGG, AAAGTAGGAGCGCCCCCTGCTGG, which resulted in a Exon Deletion. (J:265051) Inheritance:    Not Specified

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Brinp2 Mutation:	35 strains or lines available

Original:	J:265051 MGI and IMPC, MGI Load of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC). Database Release. 2018-2023;
All:	1 reference(s)