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

Symbol:	Slc17a8tm1(cre)Lowl
Name:	solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8; targeted mutation 1, Bradford B Lowell
MGI ID:	MGI:5471228
Synonyms:	CreB, Vglut3-cre, Vglut3-ires-Cre, VT3Cre
Gene:	Slc17a8  Location: Chr10:89409882-89457111 bp, - strand  Genetic Position: Chr10, 44.99 cM
Alliance:	Slc17a8tm1(cre)Lowl page

Germline Transmission:	Earliest citation of germline transmission: J:193903
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified

Allele Type:    Targeted (Recombinase) Mutation:    Insertion   Slc17a8tm1(cre)Lowl expression driven by 1 gene Knock-in expression driven by: Organism Driver Gene Note mouse Slc17a8 (MGI:3039629)     An IRES-cre cassette was inserted into the 3' UTR of the Slc17a8 gene. (J:193903, J:237954, J:243768)

Activity:	Tissue activity of this recombinase allele
Driver:	Slc17a8 (mouse) Summary of all recombinase alleles driven by Slc17a8. Alliance mouse Slc17a8 gene page

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 Slc17a8 Mutation:	40 strains or lines available

Original:	J:193903 Lou S, et al., Runx1 controls terminal morphology and mechanosensitivity of VGLUT3-expressing C-mechanoreceptors. J Neurosci. 2013 Jan 16;33(3):870-82
All:	14 reference(s)