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

Symbol:	Akap9tm1e(KOMP)Wtsi
Name:	A kinase anchor protein 9; targeted mutation 1e, Wellcome Trust Sanger Institute
MGI ID:	MGI:4363691
Gene:	Akap9  Location: Chr5:3977410-4130204 bp, + strand  Genetic Position: Chr5, 2.26 cM, cytoband A2
IMPC:	Akap9 gene page

Mutant Cell Lines:	EPD0033_5_A01, EPD0033_5_E01, EPD0033_5_F03, EPD0033_5_G01
Germline Transmission:	Unknown
Parent Cell Line:	JM8.F6 (ES Cell)
Strain of Origin:	C57BL/6N
Project Collection:	KOMP-CSD

Allele Type:    Targeted (Null/knockout, Reporter) Mutation:    Insertion     Vector: L1L2_gt0   Mutation details: The L1L2_gt0 cassette was inserted at position 4018123 of Chromosome 5 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. Insertion of this cassette creates a reporter knockout mouse. Cre expression will remove the neomycin selection cassette. Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml (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 Akap9 Mutation:	180 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)