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Smad5tm1Zuk
Targeted Allele Detail
Summary
Symbol: Smad5tm1Zuk
Name: SMAD family member 5; targeted mutation 1, Martin M Matzuk
MGI ID: MGI:1857666
Synonyms: smad5m1
Gene: Smad5  Location: Chr13:56850823-56890190 bp, + strand  Genetic Position: Chr13, 30.12 cM
Alliance: Smad5tm1Zuk page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:53293
Parent Cell Line:  AB2.1 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1b-m2
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA PGK-hprt expression cassette replaced exon 2 and its flanking sequences. In addition, a transcriptional terminator sequence was introduced into intron 1. (J:53293)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 148 assay results
1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 13 anatomical structure(s)
Tumor Data
List all tumor models in MMHCdb carrying Smad5tm1Zuk
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 Smad5 Mutation:  23 strains or lines available
References
Original:  J:53293 Chang H, et al., Smad5 knockout mice die at mid-gestation due to multiple embryonic and extraembryonic defects. Development. 1999 Apr;126(8):1631-42
All:  14 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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Funding Information
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory