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Med12tm1Hsch
Targeted Allele Detail
Summary
Symbol: Med12tm1Hsch
Name: mediator complex subunit 12; targeted mutation 1, Heinrich Schrewe
MGI ID: MGI:4839484
Synonyms: Med12hypo
Gene: Med12  Location: ChrX:100317636-100341071 bp, + strand  Genetic Position: ChrX, 43.91 cM, cytoband C2
Alliance: Med12tm1Hsch page
Mutation
origin
Mouse Generated:  Earliest citation of chimera generation: J:166040
Parent Cell Line:  G4 (ES Cell)
Strain of Origin:  (129S6/SvEvTac x C57BL/6NCrl)F1
Mutation
description
Allele Type:    Targeted
Mutation:    Insertion
 
Mutation detailsOne loxP site was inserted in the 5'UTR of exon 1 while a second loxP site, followed by an FRT flanked neomycin cassette in reverse orientation, was inserted in intron 7. Gene expression was reduced 90%. (J:166040)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 8 anatomical structure(s)
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 Med12 Mutation:  6 strains or lines available
References
Original:  J:166040 Rocha PP, et al., Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling. Development. 2010 Aug;137(16):2723-31
All:  1 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
10/29/2024
MGI 6.24
The Jackson Laboratory