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

Symbol:	Nr4a2tm1(KOMP)Wtsi
Name:	nuclear receptor subfamily 4, group A, member 2; targeted mutation 1, Wellcome Trust Sanger Institute
MGI ID:	MGI:4419243
Synonyms:	2210008N01Riktm1(KOMP)Wtsi
Gene:	Nr4a2  Location: Chr2:56996845-57014018 bp, - strand  Genetic Position: Chr2, 31.66 cM
IMPC:	Nr4a2 gene page

Mutant Cell Lines:	EPD0417_3_B10, EPD0417_3_D09, EPD0417_3_D11
Germline Transmission:	Unknown
Parent Cell Line:	JM8A3.N1 (ES Cell)
Strain of Origin:	C57BL/6N-Atm1Brd
Project Collection:	KOMP-CSD

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion     Vector: L1L2_Bact_P   Mutation details: The insertion of the L1L2_Bact_P cassette created a deletion of size 2220 starting at position 57000544 and ending at position 57002764 of Chromosome 2 (Genome Build GRCm39). This deletion results in the removal of functionally critical exon(s). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. (J:148605, J:173534)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 0 strains available      Cell Lines: 1 line available
Carrying any Nr4a2 Mutation:	40 strains or lines available

Original:	J:148605 Wellcome Trust Sanger Institute, Alleles produced for the KOMP project by the Wellcome Trust Sanger Institute. MGI Direct Data Submission. 2009;
All:	2 reference(s)