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Slc19a2tm1Ejn
Targeted Allele Detail
Nomenclature
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: Chr1:164249046-164265385 bp, + strand  Genetic Position: Chr1, 71.56 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:101675
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
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:  6 strains or lines available
References
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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/15/2014
MGI 5.18
The Jackson Laboratory