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Slc19a2tm1Gelb
Targeted Allele Detail
Nomenclature
Symbol: Slc19a2tm1Gelb
Name: solute carrier family 19 (thiamine transporter), member 2; targeted mutation 1, Bruce D Gelb
MGI ID: MGI:2429761
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:79974
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Insertion
 
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Slc19a2 Mutation:  6 strains or lines available
References
Original:  J:79974 Oishi K, et al., Targeted disruption of Slc19a2, the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice. Hum Mol Genet. 2002 Nov 1;11(23):2951-60
All:  4 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
08/12/2014
MGI 5.19
The Jackson Laboratory