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

Symbol:	Slc19a3tm1Said
Name:	solute carrier family 19, member 3; targeted mutation 1, Hamid M Said
MGI ID:	MGI:4948864
Synonyms:	Slc19a3tm1Igl, Slc19a3tm1Itl
Gene:	Slc19a3  Location: Chr1:82990244-83016169 bp, - strand  Genetic Position: Chr1, 42.65 cM
Alliance:	Slc19a3tm1Said page

Germline Transmission:	Earliest citation of germline transmission: J:170952
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: A neo cassette replaced exons 1 and 2. The absence of protein expression was confirmed by western blot analysis on intestine extracts. (J:170952)

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

In Structures Affected by this Mutation:

6 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Slc19a3 Mutation:	45 strains or lines available

Original:	J:170952 Reidling JC, et al., Impaired intestinal vitamin B1 (thiamin) uptake in thiamin transporter-2-deficient mice. Gastroenterology. 2010 May;138(5):1802-9
All:	3 reference(s)