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

Symbol:	Del(1Fmo4-Fmo2)1Eshe
Name:	deletion, Chr 1, Elizabeth A Shephard 1
MGI ID:	MGI:5487815
Synonyms:	Del1Eshe, Del(Fmo4-Fmo2)1Eshe, Fmo1-Fmo2-Fmo4-
Gene:	Del(1Fmo4-Fmo2)1Eshe  Location: unknown  Genetic Position: Chr1, Syntenic

Germline Transmission:	Earliest citation of germline transmission: J:196270
Parent Cell Line:	E14TG2a (ES Cell)
Strain of Origin:	129P2/OlaHsd

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intergenic deletion, Intragenic deletion   Del(1Fmo4-Fmo2)1Eshe involves 4 genes/genome features (Fmo4, Fmo1, Gm32197 ...) View all   Mutation details: Cre-mediated recombination between Fmo2tm1Eshe and Fmo4tm1Eshe removed exons 2 through 9 of Fmo2, the entire Fmo1 gene and exons 1 through 7 of Fmo4. (J:196270)

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

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 Del(1Fmo4-Fmo2)1Eshe Mutation:	0 strains or lines available

Original:	J:196270 Hernandez D, et al., Deletion of the mouse Fmo1 gene results in enhanced pharmacological behavioural responses to imipramine. Pharmacogenet Genomics. 2009 Apr;19(4):289-99
All:	4 reference(s)