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Smad2tm1.1Epb
Targeted Allele Detail
Summary
Symbol: Smad2tm1.1Epb
Name: SMAD family member 2; targeted mutation 1.1, Erwin P Bottinger
MGI ID: MGI:3703160
Synonyms: Smad2f
Gene: Smad2  Location: Chr18:76374651-76444034 bp, + strand  Genetic Position: Chr18, 51.42 cM
Alliance: Smad2tm1.1Epb page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:119642
Parent Cell Line:  WW6 (ES Cell)
Strain of Origin:  STOCK 129/Sv and C57BL/6J and SJL
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsExon 2, which contains the ATG, remained flanked by loxP sites following in vivo cre-mediated recombination by crossing floxed mice with cre mice. A floxed pgk-neomycin resistance cassette was removed from the locus. (J:119642)
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Smad2 Mutation:  52 strains or lines available
References
Original:  J:119642 Ju W, et al., Deletion of Smad2 in mouse liver reveals novel functions in hepatocyte growth and differentiation. Mol Cell Biol. 2006 Jan;26(2):654-67
All:  22 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
11/12/2024
MGI 6.24
The Jackson Laboratory