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Slc16a2tm1.1Sref
Targeted Allele Detail
Summary
Symbol: Slc16a2tm1.1Sref
Name: solute carrier family 16 (monocarboxylic acid transporters), member 2; targeted mutation 1.1, Samuel Refetoff
MGI ID: MGI:3687950
Synonyms: Mct8-
Gene: Slc16a2  Location: ChrX:102741020-102865589 bp, - strand  Genetic Position: ChrX, 46.29 cM
Alliance: Slc16a2tm1.1Sref page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:113732
Parent Cell Line:  E14TG2a.4 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsExon 3 was removed upon the self-excising activity of the floxed cre recombinase in Slc16a2tm1Sref mice. (J:113732)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 59 assay results
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Slc16a2 Mutation:  9 strains or lines available
References
Original:  J:113732 Dumitrescu AM, et al., Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice. Endocrinology. 2006 Sep;147(9):4036-43
All:  16 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
05/28/2024
MGI 6.13
The Jackson Laboratory