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

Symbol:	Apomtm1Stf
Name:	apolipoprotein M; targeted mutation 1, Markus Stoffel
MGI ID:	MGI:3806679
Gene:	Apom  Location: Chr17:35347973-35350777 bp, - strand  Genetic Position: Chr17, 18.59 cM, cytoband B2
Alliance:	Apomtm1Stf page

Germline Transmission:	Earliest citation of germline transmission: J:138581
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: All the coding exons were replaced with a neo cassette. The absence of protein expression was confirmed by western blot analysis on plasma extracts. (J:138581)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

1 anatomical structure(s)

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:	9 strains or lines available

Original:	J:138581 Wolfrum C, et al., Foxa2 activity increases plasma high density lipoprotein levels by regulating apolipoprotein M. J Biol Chem. 2008 Jun 13;283(24):16940-9
All:	1 reference(s)