About   Help   FAQ
Apomtm1Cchr
Targeted Allele Detail
Nomenclature
Symbol: Apomtm1Cchr
Name: apolipoprotein M; targeted mutation 1, Christina Christoffersen
MGI ID: MGI:3772574
Synonyms: ApoM-
Gene: Apom  Location: Chr17:35128997-35132050 bp, - strand  Genetic Position: Chr17, 18.59 cM, cytoband B2
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:130647
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA neo cassette was inserted into exon 2 deleting 39 bp of endogenous sequence. The absence of protein expression was confirmed by western blot analysis on serum. (J:130647)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
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 Apom Mutation:  5 strains or lines available
References
Original:  J:130647 Christoffersen C, et al., Effect of apolipoprotein M on high density lipoprotein metabolism and atherosclerosis in low density lipoprotein receptor knock-out mice. J Biol Chem. 2008 Jan 25;283(4):1839-47
All:  6 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
09/19/2017
MGI 6.10
The Jackson Laboratory