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

Symbol:	Slc27a5tm1Asta
Name:	solute carrier family 27 (fatty acid transporter), member 5; targeted mutation 1, Andreas Stahl
MGI ID:	MGI:3757682
Gene:	Slc27a5  Location: Chr7:12722273-12732119 bp, - strand  Genetic Position: Chr7, 7.71 cM
Alliance:	Slc27a5tm1Asta page

Germline Transmission:	Earliest citation of germline transmission: J:124917
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	129/Sv

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion   Mutation details: Exon 1 was replaced with a promoterless nuclear localization signal-tagged lacZ/PGK-neo cassette. The absence of protein product was confirmed by western blot analysis on liver lysates. (J:124917)

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

In Structures Affected by this Mutation:

4 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 Slc27a5 Mutation:	31 strains or lines available

Original:	J:124917 Doege H, et al., Targeted deletion of FATP5 reveals multiple functions in liver metabolism: alterations in hepatic lipid homeostasis. Gastroenterology. 2006 Apr;130(4):1245-58
All:	3 reference(s)