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

Symbol:	Slc19a2tm1Ejn
Name:	solute carrier family 19 (thiamine transporter), member 2; targeted mutation 1, Ellis J Neufeld
MGI ID:	MGI:3605162
Synonyms:	Slc19a2-
Gene:	Slc19a2  Location: Chr1:164076615-164092954 bp, + strand  Genetic Position: Chr1, 71.56 cM
Alliance:	Slc19a2tm1Ejn page

Germline Transmission:	Earliest citation of germline transmission: J:101675
Parent Cell Line:	J1 (ES Cell)
Strain of Origin:	129S4/SvJae

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: A neo cassette replaced sequence spanning from intron 2 to intron 5. Northern blot and RT-PCR confirmed absence of transcript in various tissues. (J:101675)

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 Slc19a2 Mutation:	33 strains or lines available

Original:	J:101675 Fleming JC, et al., Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2. Mol Genet Metab. 2003 Sep-Oct;80(1-2):234-41
All:	3 reference(s)