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Slc22a2tm1Ahs
Targeted Allele Detail
Nomenclature
Symbol: Slc22a2tm1Ahs
Name: solute carrier family 22 (organic cation transporter), member 2; targeted mutation 1, Alfred H Schinkel
MGI ID: MGI:2680270
Synonyms: Oct2-
Gene: Slc22a2  Location: Chr17:12584189-12628465 bp, + strand  Genetic Position: Chr17, 8.61 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:86270
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 1, as well as upstream sequence, was replaced with a neomycin selection cassette inserted by homologous recombination. Exon 1 encoded the start codon, the putative TMD1 domain, and the extracellular loop between the putative TMD1 and TMD2 domains. Transcript was undetected in homozygous mutant mice by Northern blot analysis of total kidney RNA. (J:86270)
Phenotypes
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View phenotypes for all genotypes (concatenated display).
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 Slc22a2 Mutation:  20 strains or lines available
References
Original:  J:86270 Jonker JW, et al., Deficiency in the organic cation transporters 1 and 2 (Oct1/Oct2 [Slc22a1/Slc22a2]) in mice abolishes renal secretion of organic cations. Mol Cell Biol. 2003 Nov;23(21):7902-8
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
08/17/2016
MGI 6.05
The Jackson Laboratory