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Slc16a3tm1.1Lupel
Targeted Allele Detail
Summary
Symbol: Slc16a3tm1.1Lupel
Name: solute carrier family 16 (monocarboxylic acid transporters), member 3; targeted mutation 1.1, Luc Pellerin
MGI ID: MGI:6471733
Synonyms: MCT4f, MCT4fE3-5
Gene: Slc16a3  Location: Chr11:120839310-120849826 bp, + strand  Genetic Position: Chr11, 84.73 cM
Alliance: Slc16a3tm1.1Lupel page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:296658
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Targeted (Conditional ready)
Mutation:    Insertion
 
Mutation detailsA loxP site was inserted into intron 2 and an FRT site flanked neomycin resistance gene cassette and a second loxP site into intron 5. The neo cassette was removed through subsequent flp-mediated recombination, leaving a conditional-ready allele with exon 3-5 floxed. (J:296658)
Phenotypes
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View phenotypes and curated references 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: 0 strains available      Cell Lines: 0 lines available
Carrying any Slc16a3 Mutation:  25 strains or lines available
References
Original:  J:296658 Boucanova F, et al., Disrupted function of lactate transporter MCT1, but not MCT4, in Schwann cells affects the maintenance of motor end-plate innervation. Glia. 2020 Jul 20;
All:  4 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory