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Smad7tm1.1Shou
Targeted Allele Detail
Summary
Symbol: Smad7tm1.1Shou
Name: SMAD family member 7; targeted mutation 1.1, Weinian Shou
MGI ID: MGI:3839577
Synonyms: Smad7deltaMH2
Gene: Smad7  Location: Chr18:75500600-75529006 bp, + strand  Genetic Position: Chr18, 51.06 cM, cytoband E2
Alliance: Smad7tm1.1Shou page
Defects of cardiac development in Smad7tm1.1Shou/Smad7tm1.1Shou mice

Show the 4 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:145777
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsGerm line, cre mediated recombination removed the 5' portion of exon 4. The entire exon 4 codes for the MH2 domain. RT-PCR confirmed the lack of transcripts containing exon 4. (J:145777)
Generation of the Smad7tm1Shou and Smad7tm1.1Shou alleles
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 7 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 Smad7 Mutation:  53 strains or lines available
References
Original:  J:145777 Chen Q, et al., Smad7 is required for the development and function of the heart. J Biol Chem. 2009 Jan 2;284(1):292-300
All:  2 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
12/10/2024
MGI 6.24
The Jackson Laboratory