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

Symbol:	Apomtm1(KOMP)Vlcg
Name:	apolipoprotein M; targeted mutation 1, Velocigene
MGI ID:	MGI:4399585
Gene:	Apom  Location: Chr17:35347973-35350777 bp, - strand  Genetic Position: Chr17, 18.59 cM, cytoband B2
Alliance:	Apomtm1(KOMP)Vlcg page
IMPC:	Apom gene page

Mutant Cell Lines:	13369A-A3, 13369A-A6, 13369A-B4, 13369A-B5, 13369A-B6, 13369A-G7
Germline Transmission:	Earliest citation of germline transmission: J:204812
Parent Cell Line:	VGB6 (ES Cell)
Strain of Origin:	C57BL/6NTac
Project Collection:	KOMP-Regeneron

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion     Vector: ZEN-Ub1   Mutation details: The insertion of Velocigene cassette ZEN-Ub1 created a deletion of size 2657bp between positions 35348040-35350696 of Chromosome 17 (Build GRCm39). (J:136110)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 1 line available
Carrying any Apom Mutation:	9 strains or lines available

Original:	J:136110 Velocigene, Alleles produced for the KOMP project by Velocigene (Regeneron Pharmaceuticals). MGI Direct Data Submission. 2008;
All:	2 reference(s)