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

Symbol:	Slc17a7tm1Bros
Name:	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7; targeted mutation 1, Nils Brose
MGI ID:	MGI:3051945
Synonyms:	Slc17a7tm1Rmnd, VGLUT1-
Gene:	Slc17a7  Location: Chr7:44813373-44825566 bp, + strand  Genetic Position: Chr7, 29.16 cM
Alliance:	Slc17a7tm1Bros page

Germline Transmission:	Earliest citation of germline transmission: J:89958
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	129

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: The coding region between the ATG and the fifth coding exon was replaced with a synaptobrevin 2-enhanced yellow fluorescent protein minigene and a floxed neo. Southern blot and PCR confirmed successful targeting. Expression of the EYFP was not detected. (J:89958)

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

In Structures Affected by this Mutation:

2 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 Slc17a7 Mutation:	39 strains or lines available

Original:	J:89958 Wojcik SM, et al., An essential role for vesicular glutamate transporter 1 (VGLUT1) in postnatal development and control of quantal size. Proc Natl Acad Sci U S A. 2004 May 4;101(18):7158-63
All:	14 reference(s)